Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 13587575 | HCID 13587575 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20251456 | HCID 20251456 | 95.3% |
Reaction Steps
To a mixture of 40 grams of 1-butyl 3,4,4,6-tetramethyl 1,2,3,4-tetrahydropyrimidine prepared as described in example 7, and 177 grams of absolute ethanol was added over a 1/2 hour period 4.7 grams of sodium hydribodorate. The reaction mixture was stirred for 18 hours and the ethanol evaporated under diminished pressure. To the resulting product was added water and stirring was continued for 24 hours. The organic layer was separated, dissolved in ether, and the ethereal solution washed with diminished pressure to yield 38.5 grams of 1-butyl 3,4,4,6-tetramethyl hexahydropyrimidine. C13 n.m.r., solvent CDCl3 ; ref. T.M.S.; ##STR13## As described above the following substituted 1,2,3,4-tetrahydropyrimidines of the general structure: ##STR14## were prepared, and are listed in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04281126 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-e90e61d66e6547f196a56386d41aa8f1 |
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| Source note | uspto-grants-1981_07 |
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