HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Diphenylacetone → 3-Diphenylmethyl-2,3,6,7,-tetrahydro-5H-thiazolo[3,2-a]pyrimidin-3-ol hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Diphenylacetone | HCID 69907 | — |
| Reactant | Tetrahydropyrimidine-2-thione | HCID 2723785 | — |
| Reactant | 3-Bromo-1,1-diphenylacetone | HCID 2794635 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Diphenylmethyl-2,3,6,7,-tetrahydro-5H-thiazolo[3,2-a]pyrimidin-3-ol hydrobromide | HCID 20495713 | — |
Reaction Steps
A 2.1 g. portion of 1,1-diphenyl-2-propanone is converted to 1-bromo-3,3-diphenyl-2-propanone by the procedure of Example 22. The 1-bromo-3,3-diphenyl-2-propanone is dissolved in 15 ml. of acetone and added to a boiling mixture of 0.80 g. of tetrahydro-2-pyrimidinethione in 70 ml. of acetone. This mixture is allowed to stand for 48 hours and the resulting solid is collected by filtration, giving the desired product, m.p. 196°-198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04340734 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-0b8f9b50bb0b4930bb83163627527d3d |
| Source note | uspto-grants-1982_07 |