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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911541Generated: October 30, 2026

Chlorotrimethylsilane → HCID 61056428, compound

https://huagongshe.com/reaction/1911541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 77543566HCID 77543566—
SolventTetrahydrofuranHCID 8028—
ProductHCID 61056428HCID 6105642873%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred 2 M LiBH4 solution (16.22 ml) at r.t. in THF under an argon atmosphere was added chlorotrimethylsilane (5.47 ml) over 2 min. The white suspension was cooled to 0° C. and (RS)-(2-amino-2-(2,4-difluoro-phenyl)-propionic acid hydrochloride (2.57 g) was added portionwise over 5 min. The ice bath was removed and the compact off-white suspension was stirred at r.t. for 20 h. The mixture was cooled again to 0° C. and treated carefully with methanol (15 ml). The mixture was stirred at r.t. for 30 min, filtered and the cake was washed with MeOH. The filtrate was concentrated. The crude product was purified by column chromatography (silica gel; gradient: CH2Cl2->CH2Cl2/MeOH 9:1) to give (RS)-2-amino-2-(2,4-difluoro-phenyl)-propan-1-ol (1.47 g, 73%) as colorless viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604061B2
Source datasetuspto-grants-2013_12
ORD IDord-2d9383f2c1a7408dab3467d66fb1aac8
Source noteuspto-grants-2013_12