{"title":"ti - clisen缩合法合成1-甲酰基环丙烷羧酸甲酯","authors":"Yuichiro Ashida","doi":"10.1002/0471264229.os093.21","DOIUrl":null,"url":null,"abstract":"A. Methyl 4-chloro-2-formylbutanoate (1). An oven-dried 500-mL, threenecked (24/40), round-bottomed flask equipped with a Teflon-coated magnetic stirring bar (egg-shaped, 32 mm length x 15 mm diameter), an internal thermometer, a 50-mL pressure-equalizing addition funnel fitted with a nitrogen inlet (central neck), and a second 60-mL pressure-equalizing addition funnel is charged with methyl 4-chlorobutanoate (12 mL, 13.7 g, 100 mmol, 1 equiv) (Notes 1 and 2), HCO2Me (18 mL, 18 g, 300 mmol, 3 equiv) (Note 3), and CH2Cl2 (100 mL) (Notes 4 and 5) (Figure 1). The stirred solution is immersed in an ice bath, cooling the internal temperature to 0 °C, and TiCl4 (24 mL, 41.7 g, 220 mmol, 2.2 equiv) is added dropwise through a 60-mL dropping funnel (Figure 1, right side) (Notes 6 and 7) over a period of 20 min, while maintaining the internal temperature at 5–10 °C (Note 8). A.","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":null,"pages":null},"PeriodicalIF":0.7000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Synthesis of Methyl 1-Formylcyclopropanecarboxylate utilizing Ti-Claisen Condensation\",\"authors\":\"Yuichiro Ashida\",\"doi\":\"10.1002/0471264229.os093.21\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A. Methyl 4-chloro-2-formylbutanoate (1). An oven-dried 500-mL, threenecked (24/40), round-bottomed flask equipped with a Teflon-coated magnetic stirring bar (egg-shaped, 32 mm length x 15 mm diameter), an internal thermometer, a 50-mL pressure-equalizing addition funnel fitted with a nitrogen inlet (central neck), and a second 60-mL pressure-equalizing addition funnel is charged with methyl 4-chlorobutanoate (12 mL, 13.7 g, 100 mmol, 1 equiv) (Notes 1 and 2), HCO2Me (18 mL, 18 g, 300 mmol, 3 equiv) (Note 3), and CH2Cl2 (100 mL) (Notes 4 and 5) (Figure 1). The stirred solution is immersed in an ice bath, cooling the internal temperature to 0 °C, and TiCl4 (24 mL, 41.7 g, 220 mmol, 2.2 equiv) is added dropwise through a 60-mL dropping funnel (Figure 1, right side) (Notes 6 and 7) over a period of 20 min, while maintaining the internal temperature at 5–10 °C (Note 8). A.\",\"PeriodicalId\":19576,\"journal\":{\"name\":\"Organic Syntheses\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2016-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Syntheses\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/0471264229.os093.21\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Syntheses","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/0471264229.os093.21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthesis of Methyl 1-Formylcyclopropanecarboxylate utilizing Ti-Claisen Condensation
A. Methyl 4-chloro-2-formylbutanoate (1). An oven-dried 500-mL, threenecked (24/40), round-bottomed flask equipped with a Teflon-coated magnetic stirring bar (egg-shaped, 32 mm length x 15 mm diameter), an internal thermometer, a 50-mL pressure-equalizing addition funnel fitted with a nitrogen inlet (central neck), and a second 60-mL pressure-equalizing addition funnel is charged with methyl 4-chlorobutanoate (12 mL, 13.7 g, 100 mmol, 1 equiv) (Notes 1 and 2), HCO2Me (18 mL, 18 g, 300 mmol, 3 equiv) (Note 3), and CH2Cl2 (100 mL) (Notes 4 and 5) (Figure 1). The stirred solution is immersed in an ice bath, cooling the internal temperature to 0 °C, and TiCl4 (24 mL, 41.7 g, 220 mmol, 2.2 equiv) is added dropwise through a 60-mL dropping funnel (Figure 1, right side) (Notes 6 and 7) over a period of 20 min, while maintaining the internal temperature at 5–10 °C (Note 8). A.