Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2,3,4-tetrahydro-6-[(E)-p-methoxy-alpha-methylstyryl]-1,1,4,4-tetramethylnaphthalene | HCID 13885425 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ro 14-6113 | HCID 6439236 | 113.5% |
Reaction Steps
3.8 g (11 mmol) of (E)-1-(4-methoxyphenyl)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)-propene from Example 1 were suspended in 50 ml of methanol saturated with hydrogen chloride, and the suspension was stirred for 20 minutes at 60° C. Thereafter, the reaction solution was poured into about 150 ml of ice water and extracted with three times 100 ml of methyl tert-butyl ether. The organic phase was washed with twice 100 ml of saturated sodium chloride solution and twice with water, dried over Na2SO4 and evaporated down to give 4 g of a solid crude product. This crude product was recrystallized from isopropanol to give 1.5 g of the title compound of melting point 138°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04714786 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-64bf0f7a76084361aa55df72c69347f3 |
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| Source note | uspto-grants-1987_12 |
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