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 | 104.7% |
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 69.0 g of the title compound were obtained as a brown oil (yield: 95.9%, GLC purity: 97.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663376 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-1d8a35ce5a6d44069183da68e97bc5f0 |
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| Source note | uspto-grants-1997_09 |
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