HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609278Generated: November 1, 2026
Thionyl Chloride → Benzoyl chloride, 4-(hexyloxy)-
https://huagongshe.com/reaction/1609278
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(Hexyloxy)benzoic acid | HCID 70834 | — |
| Product | Benzoyl chloride, 4-(hexyloxy)- | HCID 170235 | — |
Reaction Steps
In 2 ml of thionyl chloride was dissolved 1.03 g of 4-hexyloxybenzoic acid and the solution was refluxed for 1 hour. The excess thionyl chloride was distilled off and the residue was dried in vacuo to give 4-hexyloxybenzoyl chloride. Separately, 1.00 g of 2-(2-aminophenylthio)benzonitrile and 0.89 g of triethylamine were dissolved in 10 ml of ether and while the solution was stirred with ice-cooling, a solution of the above 4-hexyloxybenzoyl chloride in 5 ml of ether was added. The mixture was stirred overnight. Next morning, water and an aqueous solution of sodium hydrogen carbonate were added in the order mentioned and the resulting precipitate was extracted with ethyl acetate. The extract was dried over magnesium sulfate, the solvent was distilled off, and the residue was recrystallized from ethyl acetate-n-hexane to give 1.27 g of the title compound as white prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05399703 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-986e4d8a5c3042a1ab61fcb827496913 |
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| Source note | uspto-grants-1995_03 |
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