HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979558Generated: October 30, 2026
Acetyl chloride → HCID 13922843, compound
https://huagongshe.com/reaction/979558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13922842 | HCID 13922842 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13922843 | HCID 13922843 | 87% |
Reaction Steps
A solution of 5-hydroxy-2-sulfamoylbenzo[b]thiophene (4.00 g, 0.017 m) in acetone (70 ml) was cooled to -5° C., triethylamine (1.92 g, 0.019 m) was added, followed by the dropwise addition of a solution of acetyl chloride (1.49 g, 0.019 m) in acetone (10 ml) over 15 minutes, maintaining the temperature at -5° to -3° C. After stirring at -5° C. for 21/4 hours, the mixture was filtered and the solid was washed with acetone. The combined filtrate and washings were concentrated under reduced pressure, the residue was dissolved in ethyl acetate (7.5 ml) washed with water (2×20 ml), dried and evaporated under reduced pressure. The residue was crystallized from 1,2-dichloroethane to yield 4.01 g (87%) of product melting at 129°-132° C. An analytical sample melted at 131.5°-133° C. after recrystallization from 1,2-dichloroethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04668697 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-f254addc0fbe4038a0c998137867c5d2 |
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| Source note | uspto-grants-1987_05 |
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