Safe and Sustainable Industrial-Scale Production of Anhydrous Diazomethane via a Fully DCS/SIS-Controlled Continuous Flow System: Synthesis of α-Haloketones

IF 3.1 3区 化学 Q2 CHEMISTRY, APPLIED Organic Process Research & Development Pub Date : 2024-12-02 DOI:10.1021/acs.oprd.4c00449
Limin Que, Hanrong Yang, Zhigang Lin, Jie Zheng
{"title":"Safe and Sustainable Industrial-Scale Production of Anhydrous Diazomethane via a Fully DCS/SIS-Controlled Continuous Flow System: Synthesis of α-Haloketones","authors":"Limin Que, Hanrong Yang, Zhigang Lin, Jie Zheng","doi":"10.1021/acs.oprd.4c00449","DOIUrl":null,"url":null,"abstract":"Anhydrous diazomethane in nitrogen (12% v/v, moisture at &lt;0.5 g/m<sup>3</sup>) has been safely manufactured via a fully automation controlled continuous microchannel reactor on a 1500 kg per month scale while the maximum accumulation of diazomethane was less than 20 g. Treatment of <i>N</i>-methyl-<i>N</i>-nitroso-<i>p</i>-toluenesulfonamide (MNTS, diazald) with KOH generated diazomethane <i>in situ</i>, which was isolated by a custom-designed gas–liquid distributor. Subsequently, the afforded anhydrous diazomethane was used to synthesize α-haloketones, which serve as key intermediates for anti-HIV and antihypertensive drugs such as Atazanavir and Nebivolol. The entire process from TsCl to α-haloketones had been continuously operated at the ABAChem manufacturing site for more than 6 months, affording a total of 5000 kg of pure diazomethane and 15,000 kg of α-haloketones smoothly without any safety issues. The microchannel flow reactor and gas–liquid distributor were designed specifically for the process and equipped with a fully distributed control system and safety instrumented system (DCS/SIS) to ensure safety, quality, and efficiency. The wastewater and solvent had been recycled and reused, while the process mass intensity for the six chemical synthesis steps from TsCl to the corresponding α-haloketones was significantly reduced from 200 to 300 to 40–60. This production protocol paves a safer, sustainable, and expedient access to industrial-scale synthesis of α-haloketones and other intermediates useful for production of pharmaceutical and agrochemical substances involving diazomethane.","PeriodicalId":55,"journal":{"name":"Organic Process Research & Development","volume":"4 1","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Process Research & Development","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.oprd.4c00449","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Anhydrous diazomethane in nitrogen (12% v/v, moisture at <0.5 g/m3) has been safely manufactured via a fully automation controlled continuous microchannel reactor on a 1500 kg per month scale while the maximum accumulation of diazomethane was less than 20 g. Treatment of N-methyl-N-nitroso-p-toluenesulfonamide (MNTS, diazald) with KOH generated diazomethane in situ, which was isolated by a custom-designed gas–liquid distributor. Subsequently, the afforded anhydrous diazomethane was used to synthesize α-haloketones, which serve as key intermediates for anti-HIV and antihypertensive drugs such as Atazanavir and Nebivolol. The entire process from TsCl to α-haloketones had been continuously operated at the ABAChem manufacturing site for more than 6 months, affording a total of 5000 kg of pure diazomethane and 15,000 kg of α-haloketones smoothly without any safety issues. The microchannel flow reactor and gas–liquid distributor were designed specifically for the process and equipped with a fully distributed control system and safety instrumented system (DCS/SIS) to ensure safety, quality, and efficiency. The wastewater and solvent had been recycled and reused, while the process mass intensity for the six chemical synthesis steps from TsCl to the corresponding α-haloketones was significantly reduced from 200 to 300 to 40–60. This production protocol paves a safer, sustainable, and expedient access to industrial-scale synthesis of α-haloketones and other intermediates useful for production of pharmaceutical and agrochemical substances involving diazomethane.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.90
自引率
14.70%
发文量
251
审稿时长
2 months
期刊介绍: The journal Organic Process Research & Development serves as a communication tool between industrial chemists and chemists working in universities and research institutes. As such, it reports original work from the broad field of industrial process chemistry but also presents academic results that are relevant, or potentially relevant, to industrial applications. Process chemistry is the science that enables the safe, environmentally benign and ultimately economical manufacturing of organic compounds that are required in larger amounts to help address the needs of society. Consequently, the Journal encompasses every aspect of organic chemistry, including all aspects of catalysis, synthetic methodology development and synthetic strategy exploration, but also includes aspects from analytical and solid-state chemistry and chemical engineering, such as work-up tools,process safety, or flow-chemistry. The goal of development and optimization of chemical reactions and processes is their transfer to a larger scale; original work describing such studies and the actual implementation on scale is highly relevant to the journal. However, studies on new developments from either industry, research institutes or academia that have not yet been demonstrated on scale, but where an industrial utility can be expected and where the study has addressed important prerequisites for a scale-up and has given confidence into the reliability and practicality of the chemistry, also serve the mission of OPR&D as a communication tool between the different contributors to the field.
期刊最新文献
Safe and Sustainable Industrial-Scale Production of Anhydrous Diazomethane via a Fully DCS/SIS-Controlled Continuous Flow System: Synthesis of α-Haloketones Screening Platform for Immobilized Biocatalysts Utilizing Miniature Rotating Bed Reactors Optimization and Scale-Up Synthesis of a Lappaconitine Alkaloid Derivative, QG3030, as a Novel Osteoanabolic Agent Process Development to Synthesize SGD-11275 Utilizing a Pd-Catalyzed Acetamide Arylation and Gallium-Mediated Friedel–Crafts Acylation Atom-Economical and Environmentally Friendly Bts-Based Purine PNA Monomers without Base-Protecting Groups
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1