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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230847Generated: October 30, 2026

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

https://huagongshe.com/reaction/2230847

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 numberUS06426355B1
Source datasetuspto-grants-2002_07
ORD IDord-d3ea5bccc5864d02b791d201a6fa70e5
Source noteuspto-grants-2002_07