HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 3-Thiophenecarboximidic acid ethyl ester hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Thiophene-3-carbonitrile | HCID 74231 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Thiophenecarboximidic acid ethyl ester hydrochloride | HCID 12231046 | — |
Reaction Steps
To a solution of thiophene-3-carbonitrile (10 g, 9.2 mmol) in dichloromethane (100 mL) and ethanol (170 mL) at 0° C. was added acetyl chloride (114 g, 145 mmol). The reaction was allowed to slowly warm to ambient temperature and stir 16 h. The reaction mixture was then concentrated under reduced pressure to yield a solid which was triturated with diethyl ether resulting in 17.1 g of 3-thiophenecarboximidic acid ethyl ester hydrochloride as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952024B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-03b39457916d468483cf73e01c9afa5d |
| Source note | uspto-grants-2015_02 |