Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22281119 | HCID 22281119 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22281120 | HCID 22281120 | 37% |
Reaction Steps
Into a 500 ml reactor thoroughly purged with nitrogen, 16.50 ml of an ether solution containing 49.60 mmol of ethylmagnesium bromide and 10 ml of THF were introduced. To the reactor, a solution containing 12.31 g (47.20 mmol) of 2-(1-adamantyl)-4-methoxyphenol diluted with 50 ml of a THF was dropwise added at 0° C. over a period of 15 minutes. Then, 150 ml of toluene was added, and the system was heated to 95° C. to distill off about 40 ml of a mixed solution of ether and THF, whereby an opaque white slurry was obtained. After the slurry was cooled to 20° C., 3.43 g (114.30 mmol) of paraformaldehyde and 9.40 ml (67.50 mmol) of triethylamine were added, followed by stirring at 90° C. for 30 minutes. The reaction solution was allowed to cool to room temperature and then quenched with 32 ml of 18% hydrochloric acid. The organic layer was washed with 100 ml of water, 50 ml of a sodium hydrogencarbonate aqueous solution and 100 ml of a sodium chloride aqueous solution, and then concentrated. The resulting solid was purified by silica gel column chromatography to obtain 4.95 g (yield: 37%) of 3-(1-adamantyl)-5-methoxysalicylaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06962890B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-a094e47bad6a439d8ebe984ff29f0411 |
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| Source note | uspto-grants-2005_11 |
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