Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Reactant | HCID 178439169 | HCID 178439169 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178439100 | HCID 178439100 | — |
Reaction Steps
7-formyl-4-isopropyl-2-hydroxy-2,4,6-cycloheptatrien-1-one (2.00 g, 10 mmol) was dissolved in tetrahydrofuran (20 ml) and cooled to -78° C. in a dry ice/acetone bath. A solution of methyllithium the ether (1.4M, 15 ml) was added dropwise to the solution, then dry ice/acetone bath was removed and stirring was continued until the insolubles were dissolved. An aqueous saturated ammonium chloride was added to the reaction mixture and extracted with methylene chloride. The methylene chloride layer was washed with water, dried over anhydrous sodium sulfate and solvent was distilled off to give 2.18 g of 7-(α-hydroxyethyl)-4-isopropyl-2-hydroxy-2,4,6-cycloheptatrien-l-one as a reddish brown oil (yield: quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594144 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-c4a0a44a75d0409cbfac10a34001103f |
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| Source note | uspto-grants-1997_01 |
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