HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089183Generated: October 30, 2026
Hydrochloric Acid → 1-(Dibenzo[b,d]thiophen-2-yl)ethan-1-one
https://huagongshe.com/reaction/1089183
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dibenzothiophene | HCID 3023 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Dibenzo[b,d]thiophen-2-yl)ethan-1-one | HCID 312027 | — |
Reaction Steps
To a solution of 147.4 g of dibenzothiophene in 1.6 liters of carbon tetrachloride, cooled in an ice bath, was added a filtered solution of 122.7 g of anhydrous aluminum chloride in 425 ml of dichloromethane and 65.4 ml of acetyl chloride at 10° C., over 45 minutes. The mixture was stirred for 20 minutes, then a mixture of 2.5 liters of crushed ice and 500 ml of concentrated hydrochloric acid was added in one portion. This mixture was stirred vigorously until the yellow color disappeared. The aqueous layer was separated and washed in 100 ml of carbon tetrachloride. The wash was combined with the organic layer, washed with two 2 liter portions of water, dried and evaporated. The residue was crystallized from 250 ml of toluene and 750 ml of ether, giving 85.9 g of the desired product as colorless crystals, mp 107°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04965284 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-c6048bc4716741e68ab388f9241e3f78 |
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| Source note | uspto-grants-1990_10 |
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