Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Reactant | HCID 22408116 | HCID 22408116 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 67744360 | HCID 67744360 | — |
Reaction Steps
2-(4-Bromo-3-methylbenzyloxy)tetrahydropyran (1.4 g, 5 millimol) was dissolved in tetrahydrofuran (5ml), and cooled to -20° C. with methanol-water. Under nitrogen atmosphere, thereto was added 15% hexane solution (5 ml) of n-butyllithium, and in this state, the mixture was stirred for 30 minutes. Next, benzaldehyde (0.6 ml, 6 millimol) was added, and stirred for 2 hours. During this procedure, inner-temperature was raised from -20° C. to 30° C. Then, water was added, and the mixture was extracted with ethyl acetae. After washing with water and saturated aqueous sodium chloride solution, the solvent was distilled away, and the residue was separated and purified by using a silica-gel column chromatography (ethyl acetatee:n-hexane=1:5 to 1:2) to give the title compound (0.9 g, 2.9 millimol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05516777 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-6432981ac9264a4f86a0d5be0cb2fa0a |
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| Source note | uspto-grants-1996_05 |
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