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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Boc-1-methylhydrazineHCID 3748280—
Reactant3-Chloro-2-fluorophenylboronic AcidHCID 16217158—
CatalystCupric acetateHCID 8895—
Solvent1,2-DichloroethaneHCID 11—
ProductN'-(3-chloro-2-fluoro-phenyl)-N-methyl-hydrazinecarboxylic acid tert-butyl esterHCID 5794136047.2%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-6e795915622f4757beeb6008b714e0e4
Source noteuspto-grants-2009_11