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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(4-Chlorophenyl)ethylamine | HCID 67430 | — |
| Reactant | HCID 2779933 | HCID 2779933 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 2780157 | HCID 2780157 | 60.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993561B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-d91438bf270b45ae977323b3726d608e |
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| Source note | uspto-grants-2015_03 |
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