HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690140Generated: October 31, 2026
Hydrochloric Acid → 1-(2,3-Dihydro-5-benzofuranyl)ethanone
https://huagongshe.com/reaction/1690140
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Dihydrobenzofuran | HCID 10329 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2,3-Dihydro-5-benzofuranyl)ethanone | HCID 145220 | 99.3% |
Reaction Steps
2,3-Dihydrobenzofuran (10 g, 83.2 mmol) was dissolved in dichloromethane (400 mL). The resultant mixture was added sequentially with acetyl chloride (11.8 mL, 167 mmol) and aluminum chloride (33.3 g, 250 mmol) at −10° C., and stirred at −10° C. for 0.5 hour. The reaction solution was added with 5% aqueous solution of hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and brine, dried using anhydrous sodium sulfate, and concentrated in vacuo. 1-(2,3-Dihydrobenzofuran-5-yl)ethanone (13.4 g, yield 99%) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153634B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-d5880c24f4fb445da2bc0a5d577d1241 |
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| Source note | uspto-grants-2012_04 |
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