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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911537Generated: October 31, 2026

Chlorotrimethylsilane → beta-Amino-3-chlorobenzeneethanol

https://huagongshe.com/reaction/1911537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-Amino-2-(3-chlorophenyl)acetic acidHCID 290730—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
Productbeta-Amino-3-chlorobenzeneethanolHCID 1095398099.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of lithium borohydride in THF (10.5 ml, 2 M solution) under an argon atmosphere was added dropwise chlorotrimethylsilane (5.34 ml). The resulting suspension was cooled to 0° C. and amino-(3-chlorophenyl)-acetic acid (2.0 g) was added portionwise. The ice bath was removed and stirring at r.t. was then continued for 16 h. The mixture was quenched by dropwise addition of methanol (15 ml) and then concentrated in vacuo. The residue was suspended in ethyl acetate and washed with 2 N aq NaOH. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated in vacuo to afford (RS)-2-amino-2-(3-chloro-phenyl)-ethanol (1.84 g, quant.) as a yellow viscous oil. MS (ISP): 174.2 ([{37Cl}M+H]+), 172.2 ([{35Cl}M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-f8fe01c88dce4940b5387a139f0f98a5
Source noteuspto-grants-2013_12