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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187154Generated: October 30, 2026

Water → [3-Chloro-4-(1-hydroxy-ethyl)-phenyl]carbamic acid 2-trimethylsilanyl-ethyl ester

https://huagongshe.com/reaction/2187154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant(3-Chloro-4-vinyl-phenyl)-carbamic acid 2-trimethylsilanyl-ethyl esterHCID 18543726—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product[3-Chloro-4-(1-hydroxy-ethyl)-phenyl]carbamic acid 2-trimethylsilanyl-ethyl esterHCID 54096646—

Reaction Steps

(3-Chloro-4-vinyl-phenyl)-carbamic acid 2-trimethylsilanyl-ethyl ester (2.6 g) is added to a solution of mercuric acetate (3.48 g) in water (7 mL) and tetrahydrofuran (5.25 mL) and the mixture is stirred for approximately 15 hours. 3N Aqueous sodium hydroxide (8.7 mL) and a 0.5 M solution of sodium borohydride in 3N aqueous sodium hydroxide (8.7 mL) are then added and stirring is continued for 6 hours. The solution is then saturated with sodium chloride and extracted with ethyl acetate. These organic extracts are then washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. Following removal of the solvent-under reduced pressure the residue is chromatographed over silica gel (20% ethyl acetate in hexanes is used as the eluant) to provide the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407249B1
Source datasetuspto-grants-2002_06
ORD IDord-2fe0834e70524f8fb20264278c7bb303
Source noteuspto-grants-2002_06