Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20394497 | HCID 20394497 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20394492 | HCID 20394492 | 81.1% |
Reaction Steps
1-Ethoxycarbonyl-1,2,3,6-tetrahydro-2-[1-(4-methoxyphenyl)-1-methylethyl]-4-methylpyridine (3.17 g) dissolved in 10 ml of dried tetrahydrofuran was added dropwise to a suspension of 0.9 g of lithium aluminium hydride in 5 ml of dried tetrahydrofuran while stirring under cooling with ice and then the mixture was refluxed for 30 minutes. After cooling, water-containing ether (150 ml) and then 10 ml of a 30% sodium hydroxide aqueous solution was added dropwise to the mixture while stirring under cooling with ice. An diethyl ether-tetrahydrofuran layer was decanted and combined with the diethyl ether portions with which the remaining matter had been washed. The combined liquid was dried over potassium carbonate, stripped of the solvent and distilled under reduced pressure to obtain 2.1 g of 1,2,3,6-tetrahydro-2-[1-(4-methoxyphenyl)-1-methylethyl]-1,4-dimethylpyridine as a colorless viscous mass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04166174 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-9eac33f0646449f0b7f85d1d99b48ad5 |
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| Source note | uspto-grants-1979_08 |
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