HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616637Generated: October 29, 2026
Benzoyl chloride, 3-chloro- → HCID 20368321, compound
https://huagongshe.com/reaction/616637
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride, 3-chloro- | HCID 69252 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 15422638 | HCID 15422638 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 20368321 | HCID 20368321 | — |
Reaction Steps
To 200 ml. of 1,2-dichloroethane were added 10.0 g. (0.042 mole) of 3-phenyl-6-methoxybenzothiophene and 6.5 g. (0.042 mole) of 3-chlorobenzoyl chloride. The mixture was stirred and cooled to 0° C., and 5.73 g. (0.042 mole) of aluminum chloride were added. The mixture was stirred for about one hour and ice then was added. The resulting organic layer was separated from the aqueous. The aqueous layer was washed with chloroform, and the chloroform was separated and added to the organic layer. The organic layer then was evaporated, and to the resulting residue were added 250 ml. of methanol and 15 ml. of 5N sodium hydroxide. The mixture was refluxed for 30 minutes and evaporated. The residue was recrystallized from methanol to obtain the title compound, m.p. 105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04075227 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-a28d64416f574db4884450a520c8a978 |
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| Source note | uspto-grants-1978_02 |
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