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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396115Generated: October 29, 2026

Water → tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamate

https://huagongshe.com/reaction/396115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantL-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
ReactantPotassium bisulfateHCID 516920—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Producttert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 104275—

Reaction Steps

The Weinreb amide of BocLeucine was dissolved in dry Et2O and added by cannula to an Et2O suspension of an equimolar amount of LiAlH4 at 0° C. After stirring for one hour, the reaction flask was removed from 0° C. and allowed to warm to room temperature. After a reaction time of 80 minutes, an aqueous solution of KHSO4, (2 equiv. of KHSO4, 5 ml H2O/mmnol of Weinreb amide) was added slowly while stirring. The aqueous phase was extracted with Et2O and the confined Et2O phases were washed with 3N HCl, saturated NaHCO3, and saturated NaCl. After drying (MgSO4,) and rotary evaporation, the oil was found to contain one compound by thin layer chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608030B1
Source datasetuspto-grants-2003_08
ORD IDord-31cc8d91fbfb4ab7a9b136af864b1a7b
Source noteuspto-grants-2003_08