Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl Methanesulfonate | HCID 6113 | — |
| 반응물 | Diethyl chlorophosphate | HCID 13139 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | Ethyl (diethoxyphosphoryl)methanesulfonate | HCID 10934205 | 70% |
반응 단계
A solution of ethyl methanesulfonate (4.27 mL, 40.3 mmol) in 100 mL of dry THF was treated at -78° C. with 19.3 mL (44.4 mmol) of n-BuLi in hexane. After 15 min. diethyl chlorophosphate (3.30 ml, 22.2 mmol) was added. The solution was kept at -78° C. for 0.5 h and allowed to stay at -50° C. for 1 h. Saturated ammonium chloride (75 mL) was added to the solution and the mixture warmed to room temperature. The mixture was concentrated (THF removed), diluted with water and extracted with methylene chloride (3×70 mL). The combined organic fractions were dried (MgSO4), concentrated and purified by distillation to yield 3.86 g (70%) of title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05470845 |
| 출처 데이터셋 | uspto-grants-1995_11 |
| ORD ID | ord-33529eec5d4f4ebf99ed1915cc5ec481 |
| 출처 메모 | uspto-grants-1995_11 |