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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479195Generated: November 2, 2026

Methanesulfonyl chloride → HCID 86712574, compound

https://huagongshe.com/reaction/1479195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 10536881HCID 10536881—
SolventDichloromethaneHCID 6344—
ProductHCID 86712574HCID 86712574100.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408850B2
Source datasetuspto-grants-2016_08
ORD IDord-fcde2429aeba4410bb6764487229f773
Source noteuspto-grants-2016_08