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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192411Generated: November 3, 2026

Chlorotrimethylsilane → HCID 67437266, compound

https://huagongshe.com/reaction/2192411

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 numberUS08329709B2
Source datasetuspto-grants-2012_12
ORD IDord-f736bc4da247459a986a74b5907f985c
Source noteuspto-grants-2012_12