Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | 2-tert-Butyl-6-methylphenol | HCID 16678 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 75546-54-2 | HCID 6850856 | 82% |
Reaction Steps
To the solution obtained above after hydrogen gas evolution had ceased, 45 g (0.27 mol) of 2-methyl-6-t-butylphenol were added, and then heated under reduced pressure, thereby 15 g (0.47 mol) of methanol were removed from the reaction system. Then, 15.9 g (0.27 mol) of allyl alcohol and 13.5 g (0.15 mol) of toluene were added thereto. The resulting solution after the addition of toluene and allyl alcohol were transferred to a pressure container, and the atmosphere thereof was substituted with nitrogen gas, sealed and heated up to 210° C. and maintained at the same temperature for 4 hours. Thereafter the reaction mixture was cooled to room temperature and a sample thereof was analyzed by gas-chromatography. The desired product, 3-(3-t-butyl-4-hydroxy-5-methylphenyl)propanol was obtained in a yield of 82%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06717020B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-c929776bca274dc8ad0dcc94c8bc62a2 |
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| Source note | uspto-grants-2004_04 |
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