Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656615Generated: October 27, 2026

Triethylamine → (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-mesylbutanoate

https://huagongshe.com/reaction/656615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-methyl 2-(tert-butyldimethylsilyloxy)-4-hydroxybutanoateHCID 11107713—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(S)-methyl 2-(tert-butyldimethylsilyloxy)-4-mesylbutanoateHCID 86636767—

Reaction Steps

To a solution of (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-hydroxybutanoate (91c, 3.9 g, 15.7 mmol) in anhydrous dichloromethane was added triethylamine, DMAP, and mesyl chloride. The reaction was allowed to stir for 1.5 h. The reaction was quenched with saturated aqueous NH4Cl. The aqueous phase was extracted with dichlormethane and the combine organic phases were washed with brine. The organic layer was dried over anhydrous sodium sulfate and the solvent removed in vacuo to yield (S)-methyl 2-(tert-butyldimethylsilyloxy)-4-mesylbutanoate (91d, 4.9 g, 15 mmol) as a yellow oil. [M+H] calc'd for C12H26O6SSi, 327. found, 327.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071766B2
Source datasetuspto-grants-2011_12
ORD IDord-489886fa2e4b416eb0f3dd0df1198fed
Source noteuspto-grants-2011_12