HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438043Generated: October 30, 2026
Triethylamine → N'-(3-chloro-2-fluoro-phenyl)-N-methyl-hydrazinecarboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1438043
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Boc-1-methylhydrazine | HCID 3748280 | — |
| Reactant | 3-Chloro-2-fluorophenylboronic Acid | HCID 16217158 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N'-(3-chloro-2-fluoro-phenyl)-N-methyl-hydrazinecarboxylic acid tert-butyl ester | HCID 57941360 | 47.2% |
Reaction Steps
A mixture of N-methyl-hydrazinecarboxylic acid tert-butyl ester (Intermediate 1; 500 mg, 3.4 mmol), 3-chloro-2-fluorophenylboronic acid (Aldrich; 584 mg, 3.35 mmol), copper(II) acetate (621 mg, 3.4 mmol) and triethylamine (480 μL, 3.4 mmol) in 1,2-dichloroethane (4 mL) was heated in an oil bath at 50° C. for 3 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′-(3-chloro-2-fluoro-phenyl)-N-methyl-hydrazinecarboxylic acid tert-butyl ester (434 mg, 46%) as a colorless oil which 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-6e795915622f4757beeb6008b714e0e4 |
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| Source note | uspto-grants-2009_11 |
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