HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438065Generated: November 2, 2026
Triethylamine → N-benzyl-N'-(2,3-dimethyl-phenyl)-hydrazinecarboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1438065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3-Dimethylphenylboronic acid | HCID 2773395 | — |
| Reactant | N-benzyl(tert-butoxy)carbohydrazide | HCID 10799067 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-benzyl-N'-(2,3-dimethyl-phenyl)-hydrazinecarboxylic acid tert-butyl ester | HCID 57941521 | 39.6% |
Reaction Steps
A mixture of N-benzyl-hydrazinecarboxylic acid tert-butyl ester (Intermediate 27; 790 mg, 3.55 mmol), 2,3-dimethylphenylboronic acid (Aldrich; 522 mg, 3.48 mmol), copper(II) acetate (646 mg, 3.55 mmol) and triethylamine (500 μL, 3.55 mmol) in 1,2-dichloroethane (5.5 mL) was heated in an oil bath at 50° C. for 2 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 20-40% ethyl acetate/hexanes, to give N-benzyl-N′-(2,3-dimethyl-phenyl)-hydrazinecarboxylic acid tert-butyl ester (450 mg, 39%) as a yellow oil.
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-16503d8681624c049d9b7e2735ef3f49 |
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| Source note | uspto-grants-2009_11 |
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