HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479195Generated: November 2, 2026
Methanesulfonyl chloride → HCID 86712574, compound
https://huagongshe.com/reaction/1479195
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10536881 | HCID 10536881 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86712574 | HCID 86712574 | 100.6% |
Reaction Steps
To a solution of 2-(4-trifluoromethyl-benzyloxy)-ethanol (1.0 g, 4.5 mmol) in dry DCM (20 ml) and DIPEA (2.36 ml, 13.5 mmol), at 0° C., under argon atmosphere, was added methanesulfonyl chloride (421 μl, 5.4 mmol). The reaction mixture was stirred at 0° C. for 10 minutes, then the ice-bath removed and the stirring continued for 2 hours at r.t. The mixture was then diluted with 70 ml of DCM and washed with 50 ml of NaHCO3 saturated solution, 100 ml of water, 100 ml of 2N HCl and 100 ml of water, dried over sodium sulfate and evaporated to dryness affording 1.35 g (yield: quantitative) of methanesulfonic acid 2-(4-trifluoromethyl-benzyloxy)-ethyl ester as a brown oil that was used as such for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09408850B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-fcde2429aeba4410bb6764487229f773 |
|---|
| Source note | uspto-grants-2016_08 |
|---|