Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 29147-99-7 | HCID 15564094 | — |
| Reactant | HCID 54484889 | HCID 54484889 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20159861 | HCID 20159861 | — |
Reaction Steps
A solution of 2.4 g of 3-methoxy-2-(4-pentenyl)acrolein and 3.4 g of p-pentylbenzamidine hydrochloride in 30 ml of methanol was treated dropwise while stirring with a sodium methylate solution prepared from 0.55 g of sodium and 5 ml of methanol. The reaction mixture was stirred overnight at 50° C. and then neutralized (pH 5) with 3N hydrochloric acid. The solvent was distilled off and the residue was taken up in diethyl ether and water. The aqueous phase was back-extracted with diethyl ether. The organic phase was phase was washed with water, dried over sodium sulphate and concentrated. Chromatographic separation of the residue on silica gel with hexane/ethyl acetate gave 5-(4-pentenyl)-2-(p-pentylphenyl)pyrimidine as a colourless liquid; m.p. (C--I) 8.0° C., cl.p. (N--I) -4.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04621901 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-2ec93e935f7547aaa675e7a91d352f6b |
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| Source note | uspto-grants-1986_11 |
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