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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4259Generated: October 26, 2026

tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamate → 4-t-Butyloxycarbonylamino-3-hydroxy-6-methylhept-1-ene

https://huagongshe.com/reaction/4259

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 104275—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product4-t-Butyloxycarbonylamino-3-hydroxy-6-methylhept-1-eneHCID 13856048—

Reaction Steps

To a stirred 0° C. solution of Boc-leucinal (3.00 g, 13.9 mmol) in dry THF (70 ml) was added vinyl magnesium bromide (35 ml of a 1.0M solution in THF). After 5 hours, the mixture was quenched with 1.0M NH4Cl (50 ml). Most of the THF was evaporated in vacuo and the residue was extracted with ether several times. The combined extracts were washed (brine), dried (Na2SO4), filtered, and evaporated to give the desired product as a 3:2 mixture of hydroxydiastereomers in 65% field.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725584
Source datasetuspto-grants-1988_02
ORD IDord-8bab05ee85f7428ab7f581565106fcda
Source noteuspto-grants-1988_02