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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268006Generated: October 26, 2026

Tetrabutylammonium Fluoride → 1-(4-Amino-2-chlorophenyl)ethanol

https://huagongshe.com/reaction/1268006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant[3-Chloro-4-(1-hydroxy-ethyl)-phenyl]carbamic acid 2-trimethylsilanyl-ethyl esterHCID 54096646—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Amino-2-chlorophenyl)ethanolHCID 18543601—

Reaction Steps

A 1M solution of tetrabutylammonium fluoride in tetrahydrofuran (5.7 mL) is added to [3-chloro-4-(1-hydroxy-ethyl)-phenyl]-carbamic acid 2-trimethylsilanyl-ethyl ester (0.5 g) and the mixture is stirred at room temperature for approximately 3.5 hours. The solution is then concentrated under reduced pressure, dissolved in a 1:1 mixture of ethyl acetate and hexanes, washed successively with water then saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure followed by chromatography over silica gel (40% ethyl acetate in hexanes is used as the eluant) provides the product as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555561B2
Source datasetuspto-grants-2003_04
ORD IDord-64f2e2d4743f43098a31f3bde00cf864
Source noteuspto-grants-2003_04