Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 19002783 | HCID 19002783 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19002835 | HCID 19002835 | 31.1% |
Reaction Steps
353 mg of (6-methoxy-2-cyclohexylbenzo[b]thien-3-yl)[4-[2-(1-piperidinylcarbonyl)ethyl]phenyl]methanone was dissolved in 30 ml of THF, 850 mg of lithium aluminum hydride was added, and the mixture was refluxed with heating for 1 hour. A small quantity of water was added to the reaction mixture, followed by stirring, 1 ml of methanol was added, followed by stirring for 5 minutes, and 5 ml of ethyl acetate was added, followed by stirring for 5 minutes. The mixture was filtered using a super cell, the filtrate was concentrated under reduced pressure, and the resultant crude product was purified by TLC (developing solvent, chloroform:methanol=19:1) to obtain 107 mg of (6-methoxy-2-cyclohexylbenzo[b]thien-3-yl)[4-[3-(1-piperidinyl)propyl]phenyl]methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05472962 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-718cd4acb0d44c87b2dc1e80f7c74b75 |
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| Source note | uspto-grants-1995_12 |
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