HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651629Generated: November 1, 2026
Trifluoroacetic anhydride → HCID 23050245, compound
https://huagongshe.com/reaction/1651629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 23050251 | HCID 23050251 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 23050245 | HCID 23050245 | 78.2% |
Reaction Steps
5,6-Dimethoxy-benzo[b]thiophene-2-carboxamide (65 g) was suspended in pyridine (325 ml). The solution was cooled to 0° C. and treated dropwise with trifluoro acetic anhydride (185 ml) whilst maintaining the internal reaction temperature below 10° C. The mixture was then stirred at room temperature for 30 min. then cooled and treated dropwise with water (170 ml) whilst maintaining the internal temperature below 30° C. The reaction mixture was diluted with more water (800 ml), stirred and the brown solid was filtered and dried under vacuum over calcium chloride at 60° C. Recrystallisation from acetone/ether afforded 5,6-dimethoxy-benzo[b]thiophene-2-carbonitrile as a white solid (47 g), m.p. 125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04929636 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-66a70c66869b49689b79b33bb23704f5 |
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| Source note | uspto-grants-1990_05 |
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