HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489915Generated: October 31, 2026
Hydrochloric Acid → (E)-2-(fluoromethylene)-4-(p-fluorophenyl)butan-1-ol
https://huagongshe.com/reaction/1489915
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | ethyl (E)-2-(fluoromethylene)-4-(p-fluorophenyl)butyrate | HCID 15342053 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-2-(fluoromethylene)-4-(p-fluorophenyl)butan-1-ol | HCID 10943450 | — |
Reaction Steps
Cool to 0° C. a solution of diisobutylaluminum hydride (7.64 kg, 25% by weight in toluene, 13.42 mol). Add a solution of ethyl (E)-2-(fluoromethylene)-4-(p-fluorophenyl)butyrate (1.74 kg, 74.1% by weight in toluene, 5.37 mol) at such a rate that the temperature of the reaction mixture does not rise above 20° C. After the addition is complete, warm to ambient temperature. After 2 hours, cool to 0° C. Slowly, add methanol (7.73 kg) at such a rate that the temperature of the reaction mixture does not rise above 15° C. Cool to 0° C. Slowly, add water (7.96 kg) at such a rate that the temperature of the reaction mixture does not rise above 20° C. Add a concentrated aqueous solution of hydrochloric acid (7.59 kg). Warm to ambient temperature. Separate the organic layer and dry azeotropically by distillation in vacuo until the volume of the organic layer is about one half of its original volume to give the title compound as a solution in toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05679854 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-ea219fa95c5748a5816c14b26e7a522e |
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| Source note | uspto-grants-1997_10 |
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