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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245771Generated: November 1, 2026

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

https://huagongshe.com/reaction/1245771

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 numberUS07125904B2
Source datasetuspto-grants-2006_10
ORD IDord-e0e67e36d2164d3ea4716b057650cf4f
Source noteuspto-grants-2006_10