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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473338Generated: October 30, 2026

Acetic Acid → Tert-butyl 2-(1-benzhydrylazetidin-3-ylidene)hydrazinecarboxylate

https://huagongshe.com/reaction/1473338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-Butyl carbazateHCID 70091—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
SolventMethanolHCID 887—
ProductTert-butyl 2-(1-benzhydrylazetidin-3-ylidene)hydrazinecarboxylateHCID 5943653397.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

The title compound was prepared as described in WO2010079443A1. To a solution of compound 1-benzhydrylazetidin-3-one (11.7 g, 49.3 mmol) in the methanol (150 mL), tert-butyl hydrazinecarboxylate (6.51 g, 49.3 mmol) was added. Then glacial acetic acid (5.92 mL) was added dropwise at 0° C. The reaction was stirred at 25° C. for 5 h under a nitrogen atmosphere. Then the solvent was evaporated off. The residue was dissolved in dichloromethane (200 mL) and washed with water (2×500 mL). The organic part was dried over sodium sulfate, filtered and concentrated under a vacuum to give the crude tert-butyl 2-(1-benzhydrylazetidin-3-ylidene)hydrazinecarboxylate (16.9 g, 97%) as a white solid. This material was used as is for the next step. MS (ESI, positive ion) m/z (M+1): 352.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-7feb3dd3843f48b9b6893bf3ecfc538d
Source noteuspto-grants-2015_04