Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 54282796 | HCID 54282796 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53889773 | HCID 53889773 | 87.4% |
Reaction Steps
Di-isobutylaluminium hydride (1.0M in dichloromethane, 308 ml, 308 mmol) was injected into a stirred solution of methyl 7-(2,4-dichlorophenyl)-6-heptenoate (40.2 g, 140 mmol) in dichloromethane (200 ml) at -78° C. under argon. After 5 min, the solution was warmed to 0° C., stirred for 0.5 h, then cooled again to -78° C. Water (102 ml) was injected slowly, while allowing the mixture to warm to room temperature. When solid had precipitated, ethyl acetate (400 ml) was added, then excess NaHCO3, and the mixture stirred vigorously for 0.25 h. The solids were filtered off, the solvent removed under vacuum, and the residue purified by chromatography on silica gel (30-70% ether/petroleum ether 40°-60° C.) to give the title compound (31.7 g, 85%) as an oil, comprising a mixture of E and Z isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05447954 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-db02716744434c43ae10e11df4aa4720 |
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| Source note | uspto-grants-1995_09 |
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