HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437972Generated: November 3, 2026
Triethylamine → N-cyclopropyl-N'-phenyl-hydrazinecarboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1437972
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | tert-Butyl 1-cyclopropylhydrazinecarboxylate | HCID 55296944 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-cyclopropyl-N'-phenyl-hydrazinecarboxylic acid tert-butyl ester | HCID 57941480 | 45.3% |
Reaction Steps
A mixture of N-cyclopropyl-hydrazinecarboxylic acid tert-butyl ester (Intermediate 28; 0.111 g, 0.64 mmol), phenylboronic acid (Aldrich; 156 mg, 1.3 mmol), copper(II) acetate (116 mg, 0.64 mmol) and triethylamine (180 μL, 1.3 mmol) in 1,2-dichloroethane (3 mL) was heated in an oil bath at 50° C. for 16 h. The mixture was allowed to cool, and it was then adsorbed onto silica gel and purified by chromatography using an ISCO 40 g column, eluting with 5-40% ethyl acetate/hexanes, to give N-cyclopropyl-N′-phenyl-hydrazinecarboxylic acid tert-butyl ester (72 mg, 45%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622492B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-acf81872629140a6a47bcf76261b801f |
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| Source note | uspto-grants-2009_11 |
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