Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → 2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | 2-(Trimethylsilyl)ethanol | HCID 18013 | — |
| 반응물 | Benzoyl chloride, 3-(chlorosulfonyl)- | HCID 77671 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-(Trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate | HCID 86676334 | — |
반응 단계
To a mixture of 23.9 g of 3-(chlorosulfonyl)benzoyl chloride, 7.9 mL of pyridine, and 100 mL of dichloromethane was added dropwise 14 mL of 2-(trimethylsilyl)ethanol under ice-cooling, followed by stirring at room temperature for 2 hours. To the reaction mixture was added water, followed by extraction with chloroform, and the organic layer was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 29.4 g of 2-(trimethylsilyl)ethyl 3-(chlorosulfonyl)benzoate as a colorless solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09284295B2 |
| 출처 데이터셋 | uspto-grants-2016_03 |
| ORD ID | ord-fd932769b76a47e3ae3b4ecb47ed0316 |
| 출처 메모 | uspto-grants-2016_03 |