Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Chloromethyl)quinoline | HCID 20394 | — |
| Reactant | 2,2-Dibutyl-5-hydroxy-1,2,3,4-tetrahydro-1-naphthol | HCID 10516619 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | FR 110302 | HCID 164102 | 77.7% |
Reaction Steps
A mixture of (+)-2,2-dibutyl-5-hydroxy-1,2,3,4-tetrahydro-1-naphtol(138mg), 2-chloromethylquinoline(89 mg) and potassium carbonate(138 mg) in N,N-dimethylformamide(1 ml) was stirred at 70° C. for 3 hours. The cooled mixture was poured into brine(10 ml). The separated oil was extracted with brine(5 ml×3). The combined organic layers were washed with brine(5 ml), dried over magnesium sulfate and concentrated in vacuo. The residue was purified by columnchromatography on silica gel(elution by 15% ethyl acetate in hexane) to give a pale yellow syrup. The residual syrup was crystallized from methanol to yield (+)-2,2-dibutyl-5-(2-quinolylmethoxy)-1,2,3,4-tetrahydro-1naphtol(162 mg) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04965274 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-b6e24b56b23f4244b272a4042e246323 |
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| Source note | uspto-grants-1990_10 |
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