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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627261Generated: October 27, 2026

Diisobutylaluminumhydride → (S)-tert-butyl 1-methoxybut-3-en-2-yl(2-oxoethyl)carbamate

https://huagongshe.com/reaction/627261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant(S)-tert-butyl 2-(methoxy(methyl)amino)-2-oxoethyl(1-methoxybut-3-en-2-yl)carbamateHCID 89863103—
SolventDichloromethaneHCID 6344—
Product(S)-tert-butyl 1-methoxybut-3-en-2-yl(2-oxoethyl)carbamateHCID 8986309368%

Reaction Steps

To a solution of (S)-tert-butyl 2-(methoxy(methyl)amino)-2-oxoethyl(1-methoxybut-3-en-2-yl)carbamate (Intermediate 251, 3.35 g, 11.08 mmol) in dichloromethane (60 ml) at −78° C. under nitrogen was added diisobutylaluminum hydride (1.5 eq, 1.0M in dichloromethane) (16.62 ml, 16.62 mmol). The reaction mixture was stirred at that temperature for two hours. The reaction was quenched with slow addition of methanol at the low temperature and slowly warmed to ambient temperature. The reaction mixture was diluted with dichloromethane and washed with 10% aqueous potassium sodium tartrate twice, followed by water and brine. The organics were dried over sodium sulfate, filtered and concentrated. Silica gel chromatography (0%-50% ethyl acetate/hexanes) afforded the title compound as a clear oil (1.8 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309245B2
Source datasetuspto-grants-2016_04
ORD IDord-aac0c8f7e32b4be7ab66b895248a9894
Source noteuspto-grants-2016_04