HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 21162562, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Ethyl 5-(hydroxymethyl)-2-thiophenecarboxylate | HCID 24729456 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21162562 | HCID 21162562 | — |
Reaction Steps
To a suspension of ethyl 5-hydroxymethylthiophene-2-carboxylate synthesized in Production Example 72 in toluene, 212 μL of thionyl chloride was dropwise added, and the mixture was refluxed for 30 minutes. The mixture was allowed to cool down to a room temperature and stirred for one hour. After the completion of the reaction was confirmed by TLC, the solvent was distilled off. The resulting residue was used for the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365553B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-d1b09b591fe8417999c4ba3269e53045 |
| Source note | uspto-grants-2016_06 |