Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | M-Cresol | HCID 342 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21962609 | HCID 21962609 | — |
Reaction Steps
To m-Cresol (4.0 g, 37 mmol), methyl vinyl ketone (3.2 mL, 37 mmol) in chloroform (25 mL), was added diispropyl ethyl amine. The mixture was heated at reflux for 16 h, allowed to cool to room temperature and evaporated. The residue has 50% product and 50% starting material. The starting material was separated as t-butyldimethyl silyl ether. The product was isolated via plug filteration using silica gel 50% hexane/ethyl acetate. Yield 4.5 g (68%). As an alternative purification procedure, the crude reaction mixture was evaporated, dissolved in DMF (0.2M) and 0.5 equivalents of imidazole and 0.5 equivalents of tBDMSCI were added. The reaction was stirred for 3 hr at room temperature and then the solvents were removed in vacuo. To the residue was added 75 mL ethyl acetate and 75 mL water (ratio of 1/1). The ethyl acetate layer was separated and dried over Na2SO4. The solvents were removed in vacuo. The crude material was placed on a pad of silical gel and the silylated m-cresol was removed with hexanes. The product was obtained by eluting with 5-10% ethyl acetate in hexanes. The solvents were removed in vacuo to give the desired product. 1H(CDCl3):7.15 (t, 1H), 6.65-6.80(m, 2H), 4.25 (t, 2H), 2.75 (t, 2H), 2.25 and 2.35 (2 s, 3H each).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101878B1 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-c51825f579f04219a56f09ef5ea43f8c |
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| Source note | uspto-grants-2006_09 |
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