HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183643Generated: October 29, 2026
Hydrochloric Acid → 1-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-one
https://huagongshe.com/reaction/2183643
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide | HCID 22473892 | — |
| Reactant | HCID 178455855 | HCID 178455855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-one | HCID 22473690 | — |
Reaction Steps
Propylmagnesium chloride (2M solution in ether; 4.3 ml) was added under nitrogen over 15 minutes to a stirred solution of 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide (2 g) in tetrahydrofuran (25 ml) then the mixture was stirred at ambient temperature for 2.33 hours. Further propylmagnesium chloride (2M solution in ether; 0.5 ml) was added, the mixture was stirred at ambient temperature for 0.5 hours, then water (150 ml) and 5M hydrochloric acid (15 ml) were added. The product was extracted into dichloromethane (3×40 ml), the combined extracts were dried (MgSO4) and the solvents were removed in vacuo. The residue was purified by column chromatography over silica using dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to leave 1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-one (0.95 g) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900216B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-5cc97c0fdbce4ef689ec890feda21870 |
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| Source note | uspto-grants-2005_05 |
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