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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247489Generated: October 30, 2026

Water → 3-Fluoropropyl methanesulfonate

https://huagongshe.com/reaction/1247489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-Fluoro-1-propanolHCID 68042—
SolventDichloromethaneHCID 6344—
Product3-Fluoropropyl methanesulfonateHCID 24838891.6%

Reaction Steps

A solution of 3-fluoro-propan-1-ol (31.2 g, 400 mmol) in 300 mL of CH2Cl2 was treated with MsCl (55 g, 38 mL, 480 mmol, 1.2 equiv) at 0° C. The resulting reaction mixture was gradually warmed to room temperature and stirred for 1–2 hours. When 1H NMR showed the reaction was complete, the reaction mixture was treated with H2O (100 mL), and the two layers were separated. The aqueous layer was extracted with CH2Cl2 (2×100 mL). The combined organic layers were washed with H2O (3×100 mL) and dried over MgSO4. The solvent was removed in vacuo to afford the desired methanesulfonic acid 3-fluoro-propyl ester (57.2 g, 91% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129259B2
Source datasetuspto-grants-2006_10
ORD IDord-239d50fc6b1f42d98fc2668d81cb4d54
Source noteuspto-grants-2006_10