HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808206Generated: November 1, 2026
3,5-Dimethylisoxazole → HCID 57732079, compound
https://huagongshe.com/reaction/1808206
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dimethylisoxazole | HCID 9312 | — |
| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57732079 | HCID 57732079 | — |
Reaction Steps
To a solution of 3,5-dimethylisoxazole (104 g, 1.07 mol, 1 eq) in THF (1 L) cooled to −78° C. under nitrogen, a solution of lithiumdiisopropylamide (1.8M ethylbenzene in THF) (630 mL, 1.134 mol, 1.06 eq) was added dropwise. After 1 hr, a solution of 3-chlorobenzaldehyde 100 g, 0.711 mole, 0.66 eq) in THF (300 mL) was added drop wise at −78° C. The reaction mixture was allowed to warm to room temperature and stirred overnight. It was cooled to 0° C., and quenched by saturated ammonium chloride solution (130 mL). The organic layer was concentrated to dryness. Water (1 L) was added to the residue was extracted with ethyl acetate (2×1 L). Combined organic extracts were washed with brine (700 mL) dried over anhydrous sodium sulfate. Concentrated and purified by column chromatography (50% ethyl acetate in hexane) over silica gel using a mixture of ethyl acetate and hexanes as eluant. The title compound was obtained as viscous brown oil (120 g, 0.507 mol, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357711B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-7d1989c3d16245958bfcb831275ea7f9 |
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| Source note | uspto-grants-2013_01 |
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