HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510156Generated: October 31, 2026
Toluene → (E)-3-(3,4-Difluorophenyl)acrylaldehyde
https://huagongshe.com/reaction/510156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | (E)-3-(3,4-difluorophenyl)-N-methoxy-N-methyl-prop-2-enamide | HCID 71761604 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-3-(3,4-Difluorophenyl)acrylaldehyde | HCID 22077703 | 76% |
Reaction Steps
(E)-3-(3,4-Difluorophenyl)-N-methoxy-N-methyl-prop-2-enamide (100 mg, 0.440 mmol) is dissolved in dry tetrahydrofuran under inert atmosphere and the resulting solution is cooled to −78° C. A solution of diisobutylaluminum hydride in toluene (1M, 1100 μl, 1.100 mmol) is slowly added and the resulting mixture is stirred for 1 h at −78° C. The reaction is allowed to warm up to room temperature and is stirred for 1 h at this temperature. The reaction mixture is concentrated under reduced pressure and the crude product is purified by flash column chromatography on silica gel (heptane/ethyl acetate 0 to 50% as eluent) to afford the desired product as white oil (56 mg, 0.333 mmol, 76% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096599B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-192a428fd3f0476fb46a98475f13306c |
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| Source note | uspto-grants-2015_08 |
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