Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Solanesol | HCID 5477212 | — |
| Reactant | 2,3,4,5-Tetramethoxytoluene | HCID 9877764 | — |
| Catalyst | Scandium(III) triflate | HCID 2734571 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86624486 | HCID 86624486 | 124.8% |
Reaction Steps
In a 50 ml four necked flask equipped with a stirrer, thermometer, gas inlet, and a reflux condenser, under argon atmosphere 0.654 g (96.52%, 1 mmol) of solanesol were dissolved in 15 ml of n-hexane and mixed with 1.07 g (5.0 mmol) of 2,3,4,5-tetramethoxy-toluene (TMT) suspended in 7.6 ml of nitromethane. The catalyst, Sc(OTf)3 (2.5 mg, 0.005 mmol), was then added. The two-phase mixture was heated up to 50° C. (internal temperature) under stirring (400 rpm). After 16 hours reaction time the mixture was cooled down to room temperature (21° C.). The hexane layer was separated and washed two times with 4 ml (total 8 ml) of nitromethane. The hexane phase was evaporated and yielded 1.03 g of crude 1,2,3,4-tetramethoxy-5-methyl-6-((2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethyl-hexatriaconta-2,6,10,14,18,22,26,30,34-nonaenyl)-benzene (tetramethoxy-CoQ9) as a colorless oil, which was purified by column chromatography on 30 g silica (elution with n-hexane/ethyl acetate=99:1, v/v) yielding 280 mg of a colorless oil which crystallized upon standing. Yield:32%; purity 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601877B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-026379ef32834dab9e2125e3229ce894 |
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| Source note | uspto-grants-2009_10 |
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