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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223542Generated: November 1, 2026

Lithium borohydride → HCID 57454785, compound

https://huagongshe.com/reaction/2223542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 67298331HCID 67298331—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57454785HCID 57454785—

Reaction Steps

(2S)-2-Benzyloxycarbonylamino-5,5,5-trifluoropentanoic acid methyl ester from Step 2 was dissolved in dry THF (400 mL). A solution of LiBH4 (2.11 g in 100 mL of dry THF) was added dropwise with stirring and the solution was allowed to stir at ambient temperature overnight. The reaction mixture was concentrated by rotary evaporation and 400 mL of water was added. The pH was then adjusted to pH 2 by addition of concentrated HCl and then the product was extracted into ethyl acetate. The organic phase was washed two times with water, dried with MgSO4, filtered, and concentrated by rotary evaporation to yield crude (S)-(4,4,4-trifluoro-1-hydroxymethyl-butyl)-carbamic acid benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375134B2
Source datasetuspto-grants-2008_05
ORD IDord-bbe8af2ce59245729506369d223beb53
Source noteuspto-grants-2008_05