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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387537Generated: October 30, 2026

Diisobutylaluminum hydride → HCID 59564912, compound

https://huagongshe.com/reaction/387537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantTert-butyl 2,2-dimethyl-5-oxopyrrolidine-1-carboxylateHCID 54299041—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 59564912HCID 5956491297%

Reaction Conditions

Temperature-78 °C

Reaction Steps

DIBAL-H (73.6 mL, 110.4 mmol) (1.5M in Toluene) was added portionwise to a solution of tert-butyl 2,2-dimethyl-5-oxopyrrolidine-1-carboxylate (23.1 g, 108.3 mmol) in dry Et2O (200 mL) cooled to −78° C. The reaction was stirred for 1 hour at −78° C., allowed to warm to room temperature and stirred for 15 hours. The reaction was quenched with NH4OH (50 mL), stirred for 20 minutes, and then diluted with EtOAc (200 mL) and 0.5M Rochelle's Salt (100 mL). The layers were separated. The organic fraction was washed with 0.5M Rochelle's (2×100 mL), brine (100 mL), dried (MgSO4) and concentrated to an oil. The oil was taken up in a solution of p-TsOH monohydrate (2.0 g, 10.8 mmol) in MeOH (200 mL) and stirred for 15 hours at room temperature. The reaction was concentrated, taken up in EtOAc (200 mL), washed with saturated Na2CO3 (2×100 mL), brine (50 mL), dried (MgSO4) and concentrated to an oil, tert-butyl 5-methoxy-2,2-dimethylpyrrolidine-1-carboxylate (24.1 g, 97% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372842B2
Source datasetuspto-grants-2013_02
ORD IDord-e7312667e5aa40678085076d330b54ca
Source noteuspto-grants-2013_02