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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
ReactantN-benzyl(tert-butoxy)carbohydrazideHCID 10799067—
CatalystCupric acetateHCID 8895—
Solvent1,2-DichloroethaneHCID 11—
ProductN-benzyl-N'-naphthalen-2-yl-hydrazinecarboxylic acid tert-butyl esterHCID 5794140349%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622492B2
Source datasetuspto-grants-2009_11
ORD IDord-02280f0b5ef245ee858bd38297ca782b
Source noteuspto-grants-2009_11