HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl (chlorosulfonyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | (Chlorosulphonyl)acetyl chloride | HCID 77642 | — |
| Product | Methyl (chlorosulfonyl)acetate | HCID 11435213 | 95% |
Reaction Steps
To a solution of 2-(chlorosulfonyl)acetyl chloride (1 g, 5.65 mmol) in dry Et2O (5 ml) cooled to 0° C., a solution of methanol (0.286 g, 6.21 mmol) in dry Et2O (1 ml) was added dropwise. After 15 minutes, the mixture was warmed to RT and stirred for 2 hours. The solvent was evaporated and the desired compound was obtained (1 g, 5.36 mmol, 95% yield) and used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09265768B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-1723900e6a784a6b9bebf1662577a60e |
| Source note | uspto-grants-2016_02 |