Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | HCID 14649319 | HCID 14649319 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14649321 | HCID 14649321 | — |
Reaction Steps
To a solution of methyl 3-(4-ethoxyphenyl)-4,4,4-trifluorobutanoate (2.0 g, 7.2×10-3 moles) in toluene (25 cm3) at -78° C. was added one molar diisobutylaluminium hydride (7.2 ml, 7.2×10-3 moles) in toluene. The resulting solution was stirred at -78° C. for two hours before quenching the reaction by the sequential addition of acetic acid (0.48 cm3, 8.4×10-3 moles), water (1 cm3) and sodium sulphate (10 g). The resulting slurry was allowed to warm to room temperature and after a further twenty minutes stirring the solids were filtered off through a silica plug. The solvent was removed to leave a colourless oil which was characterised as the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04791139 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-0d5e833f7fe24c06b217200113c335e7 |
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| Source note | uspto-grants-1988_12 |
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