Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598885Generated: October 25, 2026

Methanesulfonyl chloride → (S)-3-(tert-butoxycarbonylamino)-4-(4-chlorophenyl)butyl methanesulfonate

https://huagongshe.com/reaction/598885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-tert-Butyl 1-(4-chlorophenyl)-4-hydroxybutan-2-ylcarbamateHCID 57950531—
SolventDichloromethaneHCID 6344—
Product(S)-3-(tert-butoxycarbonylamino)-4-(4-chlorophenyl)butyl methanesulfonateHCID 5795057094%

Reaction Steps

To a mixture of (S)-tert-Butyl 1-(4-chlorophenyl)-4-hydroxybutan-2-ylcarbamate (686 mg, 2.3 mmol) and TEA (399 μl, 2.9 mmol) in DCM (10 mL) at −8° C. was added methanesulfonyl chloride (214 μl, 2.7 mmol). The resulting mixture was stirred for 2 hours. After warming to room temperature, the mixture was diluted with DCM and washed with H2O (2×). The combined organic layers were dried over Na2SO4, filtered, and concentrated to give the product as a light yellow solid (815 mg, 94%). LCMS (API-ES) m/z: 400 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-212a2d19de924ef1afb40824f29da493
Source noteuspto-grants-2011_03