HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183601Generated: October 30, 2026
Benzo(B)Thiophene → 1-Benzo[b]thien-2-yl-1-propanone
https://huagongshe.com/reaction/2183601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzo(B)Thiophene | HCID 7221 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-Methoxy-N-methylpropionamide | HCID 11344007 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Benzo[b]thien-2-yl-1-propanone | HCID 22474213 | 80.1% |
Reaction Steps
n-Butyllithium (1.6 M solution in hexanes; 28.9 ml) was added dropwise under nitrogen at 0° C. to a stirred solution of benzo[b]thiophene (6.21 g) in ether (90 ml), then the mixture was stirred 0° C. for 15 minutes and cooled to −70° C. A solution of N-methoxy-N-methylpropionamide (5.42 g) in ether (40 ml) was added over 10 minutes, then the mixture was allowed to warm to ambient temperature and was stirred at ambient temperature for 3.5 hours. The mixture was poured into saturated aqueous ammonium chloride solution (200 ml) and ethyl acetate (100 ml) and water (50 ml) were added. The organic phase was separated, washed with saturated aqueous sodium chloride solution (150 ml), dried (Na2SO4) and the solvents were removed in vacua. The residue was triturated with petroleum ether (b.p. 40-60° C.) (25 ml) and the resulting solid was collected by filtration and dried in vacuo to give 1-(benzo[b]thiophen-2-yl)propan-1-one (7.05 g) as a colourless solid, m.p. 79-81° C.
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-fdcbc5da3ff945e88f44e5aa4bc764fe |
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| Source note | uspto-grants-2005_05 |
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