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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530649Generated: October 25, 2026

Methanol → Tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate

https://huagongshe.com/reaction/1530649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantTert-butyl 2-(1-methylpiperidin-4-ylidene)hydrazinecarboxylateHCID 21097379—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylateHCID 6831322669.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of tert-butyl 2-(1-methylpiperidin-4-ylidene)hydrazinecarboxylate (500 mg, 2.20 mmol) in THF (50 mL) was added DIBAl-H (22 mL, 22 mmol) under nitrogen atmosphere. The resulting mixture was stirred at 25° C. overnight. Methanol (5 mL) was added to quench the reaction at −78° C. After being stirred at room temperature for 1 h, water (10 mL) was added. The solid was filtered off and washed with EtOAc. The combined filtrate was partitioned and extracted with EtOAc (3×50 mL), dried over Na2SO4, and concentrated. The residue was purified by silica gel chromatography eluting with EtOAc/petroleum ether (1:10) to give tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate (350 mg, 69% yield) as a colorless oil. LCMS (ESI) m/z: 230.4 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-85c9a7c1b86540e0a58e0307bac4a0ed
Source noteuspto-grants-2015_07