HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607276Generated: October 31, 2026
4-Bromobenzoyl chloride → HCID 15029669, compound
https://huagongshe.com/reaction/1607276
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 14579737 | HCID 14579737 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 15029669 | HCID 15029669 | — |
Reaction Steps
A solution of p-bromobenzoyl chloride (1.1 gm; 5.0 mmoles) in ethylene dichloride (5 mL) was added slowly to a cooled suspension of aluminium chloride (3.3 gm; 25 mmoles) in ethylene dichloride (75 mL). After stirring for a period of 10 minutes, 3-methyl-4-hydroxy-5-propyl-7-chlorobenzofuran (0.95 gm; 4.2 mmoles) in dichloroethylene (20 mL) was added over a period of 2 minutes. The reaction mixture was stirred at room temperature for 1 hour. It was cooled with an ice-bath and ice was added slowly. When the vigorous reaction subsided, the organic layer was separated and the aqueous phase was extracted with methylene chloride. The organic phases were combined, dried (Na2SO4), and concentrated in vacuo. The residue was chromatographed on silica gel and eluted with 10% ethylacetate in hexane to yield 260 mg gm of 2-(p-bromobenzoyl-3-methyl-4-(p-bromobenzoyloxy)-5-propyl-7-chlorobenzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863958 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-7a3e44f2e7124e3f891b2cd329a9fb4c |
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| Source note | uspto-grants-1989_09 |
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