Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 20059351 | HCID 20059351 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20059356 | HCID 20059356 | 73.6% |
Reaction Steps
Diisobutylaluminum hydride (20 mL of 1M solution, 20 mmol) was added to a solution of ethyl 3,3-bis(4-fluorophenyl)-2-(1,1dimethylethyl)propionate (2.0 g, 5.8 mmol) in 20 mL of methylene chloride at -70° C. The solution was stirred at -70° C. for 4 hours and at -10° C. for 18 hours. The solution was hydrolyzed by addition of 2N hydrochloric acid. The aqueous layer was separated and extracted with methylene chloride. The combined organic portions were dried with magnesium sulfate and concentrated in vacuo. The residue was crystallized from hexane to give 1.3 g of the title compound; m.p. =106°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05011947 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-3242d77d9de64f88a3510c784a6cf5d3 |
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| Source note | uspto-grants-1991_04 |
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