HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612903Generated: October 30, 2026
Benzoyl chloride → HCID 19596611, compound
https://huagongshe.com/reaction/612903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19596640 | HCID 19596640 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19596611 | HCID 19596611 | 62% |
Reaction Steps
5-(4-Aminophenyl)-3-(2-(N-tert-butoxycarbonylamino)ethoxy)isoxazole (0.1 g) was dissolved in tetrahydrofuran (I ml), and triethylamine (0.05 ml) and benzoyl chloride (0.04 ml) were successively added dropwise thereto at 5° C. under a nitrogen atmosphere, followed by stirring of the resulting mixture at room temperature for 30 minutes. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous NaCl solution and dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=3/1) to obtain the title compound (0.08 g, 62%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06005116 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-628fe027a3bb427db6bcf7a45b1478eb |
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| Source note | uspto-grants-1999_12 |
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