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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185675Generated: October 26, 2026

Diisobutylaluminum hydride → 2,2-Bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl ester

https://huagongshe.com/reaction/1185675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant2,2-Bis(tert-butoxycarbonylamino)-4-(methoxy-methyl-carbamoyl)-butyric acid benzyl esterHCID 86648875—
SolventHexaneHCID 8058—
Product2,2-Bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl esterHCID 8664887675.2%

Reaction Steps

A solution of DIBAL (1.0 M, 14.7 mL, 14.7 mmol) in hexane was added dropwise to a solution of 2,2-bis(tert-butoxycarbonylamino)-4-(methoxy-methyl-carbamoyl)-butyric acid benzyl ester (4 g, 10.5 mmol) under an atmosphere of nitrogen at −78° C. After 2 hours the mixture was quenched with saturated ammonium chloride (30 mL) and allowed to warm to room temperature. Water (20 mL) was added, and the mixture was extracted with diethyl ether (3×50 mL). The combined organic phases were left to stand at room temperature for 15 minutes. The resulting thick gel was filtered through a pad of CELITE. The filtrate was dried over sodium sulfate, filtered and the solvent was removed under reduced pressure to provide 2,2-bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl ester (3.34 g, 7.9 mmol, 75%). This was used immediately in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669234B2
Source datasetuspto-grants-2014_03
ORD IDord-2543ffcb19ea48cab9e71f436e806698
Source noteuspto-grants-2014_03