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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879982Generated: October 29, 2026

2-(4-Chlorophenyl)ethylamine → HCID 2780157, compound

https://huagongshe.com/reaction/879982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Chlorophenyl)ethylamineHCID 67430—
ReactantHCID 2779933HCID 2779933—
SolventMethanolHCID 887—
ProductHCID 2780157HCID 278015760.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

A suspension of 0.3 g (0.89 mmol) of ethyl 7-nitro-5-(trifluoromethyl)-1,3-benzothiazole-2-carboxylate-3-oxide (the synthesis of which is described in Wagner et al., Chem. Ber., 1973, 106, 640-654 compound 4e and Bayer patent DE 2013434, example 7), in 9 ml of methanol is heated with stirring until solubilization, and then cooled to 25° C. 0.157 g (1.01 mmol) of 2-(4-chlorophenyl)ethanamine is added slowly to the solution obtained. The homogeneous reaction mixture is stirred at AT overnight. It is then concentrated under reduced pressure and the residue obtained is purified by silica column chromatography (solvent: cyclohexane/-dichloromethane from 60/40 to 0/100). 0.240 g of expected compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993561B2
Source datasetuspto-grants-2015_03
ORD IDord-d91438bf270b45ae977323b3726d608e
Source noteuspto-grants-2015_03