Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 59180529 | HCID 59180529 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59180521 | HCID 59180521 | — |
Reaction Steps
A solution of 744 mg (1.75 mmol) of methyl 4-[(3E)-2-[2-(4-cyanophenyl)ethyl]-4-(2-methoxyphenyl)but-3-en-1-yl]benzoate in 24 ml of THF and 24 ml of water is mixed with 84 mg (3.5 mmol) of lithium hydroxide and stirred at 50° C. for 12 h. After conversion is complete, the reaction solution is diluted with diethyl ether and water, and the phases are separated. The aqueous phase is acidified with 1 M hydrochloric acid and extracted with diethyl ether. The resulting organic phase is washed with sodium chloride solution, dried over sodium sulphate and evaporated. 606 mg (1.5 mmol, 97% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609727B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-93d3b0f10bc0428baab1e76580906427 |
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| Source note | uspto-grants-2013_12 |
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