Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Isophytol | HCID 10453 | — |
| Reactant | Trimethylhydroquinone | HCID 12785 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | alpha-Tocopherol | HCID 14985 | 98.6% |
Reaction Steps
To a mixture consisting of 23.3 g (0.153 mol) of 2,3,5-trimethylhydroquinone, 17.5 g (0.128 mol) of zinc chloride, 47.5 ml of hexane, 2.5 ml of n-butanol and 2.5 g of concentrated hydrochloric acid, 46.1 g (0.153 mol) of isophytol (purity: 98.3%) were added dropwise under stirring at 30°-40° C. over 3 hours. At the same temperature, the reaction mixture was stirred for additional 2 hours. After the reaction mixture was washed with 10 ml of water, the solvents were distilled off. Toluene (100 ml ) was added to the residue to dissolve the same. The resulting solution was washed successively with water, alkaline water and a saturated aqueous solution of NaCl, dried over magnesium sulfate and then concentrated under reduced pressure, whereby 65.0 g of the title compound were obtained as a brown oil (yeld: 95.9%, GLC purity: 97.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05886197 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-3f0774d4829d4040a23ea2926110f126 |
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| Source note | uspto-grants-1999_03 |
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