HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386622Generated: November 1, 2026
Dimethylformamide → 2-(4-Hexyloxyphenyl)-5-ethoxycarbonylbenzoxazole
https://huagongshe.com/reaction/1386622
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-(Hexyloxy)benzoic acid | HCID 70834 | — |
| Reactant | Benzoyl chloride, 4-(hexyloxy)- | HCID 170235 | — |
| Reactant | Ethyl 3-amino-4-hydroxybenzoate | HCID 12208891 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Oxalyl chloride | HCID 65578 | — |
| Product | 2-(4-Hexyloxyphenyl)-5-ethoxycarbonylbenzoxazole | HCID 21182488 | — |
Reaction Steps
To a suspension of 4-hexyloxybenzoic acid in oxalyl chloride (10 ml) and dichloromethane (10 ml) was added N,N-dimethylformamide (0.1 ml). The mixture was stirred at room temperature for 2 hours. The solvent was removed under reduced pressure to give crude 4-hexyloxybenzoate chloride. To a suspension of Ethyl 3-amino-4-hydroxybenzoate (733 mg) and triethylamine (1.38 ml) and 4-dimethylaminopyridine (DMAP, 10 mg) in methylene chloride (10 ml) was added the solution of 4-hexyloxybenzoyl chloride obtained above in dichloromethane (5 ml) dropwise at 10° C. The reaction mixture was stirred at 10° C. for 1.5 hours and diluted with dichloromethane (20 ml). the solution was washed with H2O (20 ml), 1N HCl aq. (20 ml×2), H2O (20 ml) and brine (20 ml) successively. The organic layer was dried over MgSO4 and the solvent was removed under reduced pressure. To the residue was added toluene (15 ml) and p-toluenesulfonic acid (10 mg). The mixture was refluxed for 6 hours and the solvent was removed under reduced pressure. The residue was triturated with acetonitrile, and precipitate was collected with filtration and dried over PO5 to give 2-(4-Hexyloxyphenyl)-5-ethoxycarbonylbenzoxazole (0.60 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265536B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-506352229fd7463aaa47c7ab5d4662d6 |
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| Source note | uspto-grants-2001_07 |
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