HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211126Generated: November 2, 2026
4-Chlorobutyryl chloride → HCID 15292528, compound
https://huagongshe.com/reaction/2211126
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 3-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepine | HCID 19375487 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15292528 | HCID 15292528 | 91.8% |
Reaction Steps
In 30 ml of dichloromethane, was dissolved 3.79 g of 3-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepine. To the solution were added 3.38 g of 4-chlorobutyryl chloride and 4.00 g of aluminum chloride. The mixture was stirred for 2 hours at room temperature (about 20° C.). The reaction mixture was poured into 50 ml of ice-water. The organic layer was separated, which was washed successively with 50 ml of 0.5N aqueous solution of sodium hydroxide and 50 ml of pure water, then dried over anhydrous sodium sulfate. The solvent was distilled off to leave 5.40 g of an oily residue. The residue was purified by means of a silica gel column chromatography (developing solvent, ethyl acetate-dichloromethane 1:1 (V/V)) to afford 2.92 g of the title compound as colorless crystals, m.p.103°-106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05462934 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-ac4ffbf5f00a44ebbdb8ca4507ca6e45 |
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| Source note | uspto-grants-1995_10 |
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