Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → Carbonic acid 1-chloroethyl ester (R)-1-methylbutyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| 반응물 | 1-Chloroethyl chloroformate | HCID 521305 | — |
| 반응물 | (2R)-pentan-2-ol | HCID 7014876 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | Carbonic acid 1-chloroethyl ester (R)-1-methylbutyl ester | HCID 86677396 | — |
반응 단계
To a mixture of 1-chloroethyl chloroformate (1.19 mL), pyridine (1.49 mL), and THF (100 mL), (R)-(−)-2-pentanol [CSA No. 31087-44-2] (1 mL) dissolved in THF (3 mL) was added at −78° C. After stirring the mixture overnight at room temperature, ethyl acetate and heptane were added to the reaction mixture. The resulting mixture was sequentially washed with 0.5 N hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution, water, and saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate. The resulting mixture was filtered, and the filtrate obtained was concentrated under reduced pressure to obtain the captioned compound (1.8 g) as a crude product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08436009B2 |
| 출처 데이터셋 | uspto-grants-2013_05 |
| ORD ID | ord-278f7c81a9bb4965b93b82b0fa33b030 |
| 출처 메모 | uspto-grants-2013_05 |