HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440402Generated: October 29, 2026
Dimethyl Sulfoxide → 3-(1-Decyl)-5-isoxazolecarboxaldehyde
https://huagongshe.com/reaction/440402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-(1-Decyl)-5-isoxazolemethanol | HCID 18372945 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(1-Decyl)-5-isoxazolecarboxaldehyde | HCID 18372911 | 82% |
Reaction Steps
To a solution of oxalyl chloride (31.7 ml) in dry dichloromethane (100 ml) cooled to -60° C., was added a solution of dimethylsulfoxide (9.8 ml) in dichloromethane (30 ml) followed by a slurry of 3-(1-decyl)-5-isoxazolemethanol (13.8 g) in dry dichloromethane (100 ml). The reaction mixture was stirred at -60° C. for 0.5 hr, quenched with triethylamine (40 ml), and allowed to warm to ambient temperature. The solution was poured into water (300 ml) and extracted with dichloromethane. The organic phases were washed with dilute citric acid, dried, and evaporated. The residue was flash chromatographed (silica, 50:1-dichloromethane:methanol). The appropriate fraction were collected and evaporated. The residue was recrystallized from ether-hexane to give 11.2 g (82%) of product, mp 46°-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05519062 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-472099c10fa340579ceed389aee7ef7b |
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| Source note | uspto-grants-1996_05 |
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