HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506280Generated: November 1, 2026
Dichloromethane → Methyl 3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylate
https://huagongshe.com/reaction/1506280
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1236188-80-9 | HCID 58374094 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylate | HCID 13508376 | 97% |
Reaction Steps
To a solution of 3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylic acid (Intermediate I-3D, 0.500 g, 1.94 mmol) in dichloromethane (5 mL) and methanol (1 mL) at room temperature was added trimethyldiazomethane (2.0 M in ether) (1.26 mL, 2.53 mmol) slowly over 5 min. The resulting reaction mixture was stirred for 30 min. The reaction mixture was diluted with dichloromethane (40 mL) and washed with brine (20 mL). The aqueous layer was extracted with dichloromethane (2×20 mL), and the organic layers were combined and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded methyl 3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylate (0.513 g, 1.89 mmol, 97% yield) as a yellow oil. The product had an HPLC ret. time=2.55 min. (condition A); LC/MS M+1=272.0; 1H NMR (400 MHz, CDCl3) δ ppm 4.07 (s, 3H), 7.47-7.56 (m, 3H), and 7.59 (d, J=7.04 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216972B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-89a36b5aca514122bf92d40b1d74e215 |
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| Source note | uspto-grants-2015_12 |
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