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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340105Generated: October 30, 2026

Chlorotrimethylsilane → HCID 67437266, compound

https://huagongshe.com/reaction/340105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium HydroxideHCID 14798—
Reactant2,4-Dichloro-L-phenylalanineHCID 2761497—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67437266HCID 67437266—

Reaction Steps

A solution of lithium tetrahydroborate (190 mg, 8.50 mmol) in THF (4 mL) was cooled to 0° C. Chlorotrimethylsilane (2.2 mL, 17 mmol) was added dropwise. The mixture was stirred for 20 minutes at room temperature and then returned to 0° C. (S)-2-amino-3-(2,4-dichlorophenyl)propanoic acid (1.00 g, 4.27 mmol) was then added. The reaction was allowed to warm up slowly to room temperature while stirring overnight. The mixture was cooled to 0° C. and quenched by slow addition of methanol (1 mL) followed by an aqueous solution of 2N sodium hydroxide (4.2 mL, 8.54 mmol). Volatiles were removed under reduces pressure. The slurry was diluted with water (5 mL) and extracted with DCM (3×15 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated to afford (S)-2-amino-3-(2,4-dichlorophenyl)propan-1-ol as a solid that was used in the next step without further purification. MS m/z 220 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895566B2
Source datasetuspto-grants-2014_11
ORD IDord-9bf5c716e79b4138bf1f2c11fd5a54a6
Source noteuspto-grants-2014_11