HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiopheneacetyl chloride → Methyl 4-chloro-5-nitro-2-(2-(thiophen-2-yl)acetamido)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiopheneacetyl chloride | HCID 162362 | — |
| Reactant | Methyl 2-amino-4-chloro-5-nitrobenzoate | HCID 15895692 | — |
| Product | Methyl 4-chloro-5-nitro-2-(2-(thiophen-2-yl)acetamido)benzoate | HCID 54055967 | 67.6% |
Reaction Steps
To a suspension of 2-amino-4-chloro-5-nitrobenzoic acid methyl ester (221 mg in 2.5 mL of dry 1,2-dichloroethane) was added a solution of thiophen-2-yl-acetyl chloride (169 mg in 3.0 mL dry 1,2-dichloroethane) and the mixture heated at reflux on an oil bath. After 18 hours, the reaction was cooled and the solvent removed in vacuo. Recrystallization of the crude product from methanol gave the title compound (230 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150522 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-3360fadb200f44918fa5a528d8f1207f |
| Source note | uspto-grants-2000_11 |