HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437879Generated: October 31, 2026
Triethylamine → N-benzyl-N'-naphthalen-2-yl-hydrazinecarboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1437879
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Naphthalen-2-yl)boronic acid | HCID 2734375 | — |
| Reactant | N-benzyl(tert-butoxy)carbohydrazide | HCID 10799067 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-benzyl-N'-naphthalen-2-yl-hydrazinecarboxylic acid tert-butyl ester | HCID 57941403 | 49% |
Reaction Steps
A mixture of N-benzyl-hydrazinecarboxylic acid tert-butyl ester (Intermediate 27; 1.21 g, 5.44 mmol), 2-naphthaleneboronic acid (Lancaster; 1.00 g, 5.8 mmol), copper(II) acetate (990 mg, 5.45 mmol) and triethylamine (1.9 mL, 13.6 mmol) in 1,2-dichloroethane (30 mL) was heated in an oil bath at 50° C. for 1.5 h. The mixture was allowed to cool, and it was then adsorbed onto silica gel and purified by chromatography using an ISCO 120 g column, eluting with 15-30% ethyl acetate/hexanes, to give N-benzyl-N′-naphthalen-2-yl-hydrazinecarboxylic acid tert-butyl ester (929 mg, 49%) as a yellow oil that solidified on standing.
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-02280f0b5ef245ee858bd38297ca782b |
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| Source note | uspto-grants-2009_11 |
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