HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Methanesulfonate | HCID 6113 | — |
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Ethyl (diethoxyphosphoryl)methanesulfonate | HCID 10934205 | 70% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05470845 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-33529eec5d4f4ebf99ed1915cc5ec481 |
| Source note | uspto-grants-1995_11 |