HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → Methoxy-2-trifluoromethylbenzothiazole-7-carboxylic acid 4-nitrophenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-Methoxy-2-trifluoromethylbenzothiazole-7-carboxylic acid | HCID 18356995 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methoxy-2-trifluoromethylbenzothiazole-7-carboxylic acid 4-nitrophenyl ester | HCID 69689660 | 74.6% |
Reaction Steps
A suspension of 4-methoxy-2-trifluoromethylbenzothiazole-7-carboxylic acid (140 mg) in dichloromethane (10ml) was treated with p-nitrophenol (72 mg), dimethylaminopyridine (catalytic) and 1-(3-dimethylaminopropyl)-3-ethyl carbodimide hydrochloride (150 mg). The mixture was stirred at room temperature for 12 hours and the reaction washed with water (10 ml). The organic layer was separated, dried over magnesium sulphate (5 g) and evaporated in vacuo. Purification by flash chromatography (eluent 50% ethyl acetate/hexane) yielded the title compound as an off-white solid (150 mg). TLC Rf 0.13 (50% ethyl acetate in heptane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313116B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-4a57574299c14853ba29b6f739adcca7 |
| Source note | uspto-grants-2001_11 |