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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | tert-Butyl carbazate | HCID 70091 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-one | HCID 3735558 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 2-(1-benzhydrylazetidin-3-ylidene)hydrazinecarboxylate | HCID 59436533 | 97.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09012443B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-7feb3dd3843f48b9b6893bf3ecfc538d |
|---|
| Source note | uspto-grants-2015_04 |
|---|