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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854701Generated: November 1, 2026

Triethylamine → [4-(Tert-butyldimethylsilanyloxy)-3-hydroxybutyl]carbamic acid tert-butyl ester

https://huagongshe.com/reaction/854701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(3,4-Dihydroxybutyl)carbamic acid tert-butyl esterHCID 11622550—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product[4-(Tert-butyldimethylsilanyloxy)-3-hydroxybutyl]carbamic acid tert-butyl esterHCID 11508015—

Reaction Steps

To a stirred solution of (3,4-dihydroxybutyl)carbamic acid tert-butyl ester (2.60 g, 12.7 mmol), triethylamine (2.03 mL, 14.50 mmol) and 4-(dimethylamino)pyridine (0.05 g, 0.4 mmol) in anhydrous dichloromethane (40 mL) at room temperature was added tert-butyldimethylchlorosilane (2.0 g, 13.17 mmol) in one portion. The resulting mixture was stirred at room temperature for 18 hours, washed with water, brine and dried over anhydrous magnesium sulfate. Filtration and concentration in vacuo gave an oil which was purified by column chromatography on silica using ethyl acetate—petroleum ether mixture as eluent to afford a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259271B2
Source datasetuspto-grants-2007_08
ORD IDord-b3b5f8e99369404b97eeb28fbe9945cd
Source noteuspto-grants-2007_08