HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465429Generated: November 1, 2026
tert-Butyl carbazate → Tert-butyl 2-[(4-bromophenyl)acetyl]hydrazinecarboxylate
https://huagongshe.com/reaction/1465429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl carbazate | HCID 70091 | — |
| Reactant | Benzeneacetic acid, 4-bromo- | HCID 74654 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 2-[(4-bromophenyl)acetyl]hydrazinecarboxylate | HCID 67029623 | 88.2% |
Reaction Steps
2-(4-Bromophenyl)acetic acid (20 g, 93 mmol), tert-butyl carbazate (14.7 g, 111 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (21.4 g, 112 mmol) and 1-hydroxybenzotriazole monohydrate (17.1 g, 112 mmol) were dissolved in dichloromethane (400 ml), and N,N-diisopropylethylamine (80 ml) was added. After stirring at room temperature for 16 hrs, the reaction mixture was washed with 1M hydrochloric acid and saturated aqueous sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentration residue was purified by silica gel column chromatography (dichloromethane:methanol=99:1→90:10) to give tert-butyl 2-[(4-bromophenyl)acetyl]hydrazinecarboxylate (27 g, yield 88%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999989B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-2db68f29434b41a68eb070d50b3bebca |
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| Source note | uspto-grants-2015_04 |
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