HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetic Acid → Benzo(B)Thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetic Acid | HCID 300 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Product | Benzo(B)Thiophene | HCID 7221 | — |
Reaction Steps
In further detail, a compound (XIV) is reacted with a benzoyl chloride in the presence of a Lewis acid (e.g. aluminum chloride or tin tetrachloride) to obtain a compound (XV). Usually, this reaction can be carried out by the use of or without a solvent (e.g. carbon disulfide or nitrobenzene) in a temperature range of room temperature to about 100° C. Then, the compound (XV) is reacted with chloroacetic acid in a temperature range of approximately 80°-130° C. to obtain benzothiophene or a derivative thereof (IIb).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464863 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-0598eb82d30840419a233bd41d48e806 |
| Source note | uspto-grants-1995_11 |