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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186003Generated: October 30, 2026

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

https://huagongshe.com/reaction/2186003

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 numberUS06403617B1
Source datasetuspto-grants-2002_06
ORD IDord-638b3b91b77847d1a28d6a542a3078b1
Source noteuspto-grants-2002_06