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HRID 1074535Erstellt: 26. Oktober 2026

1,1-Diphenylacetone → 3-Diphenylmethyl-2,3,6,7-tetrahydro-6,6-dimethyl-5H-thiazolo[3,2-a]pyrimidin-3-ol hydrobromide

https://huagongshe.com/reaction/1074535

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-DiphenylacetoneHCID 69907—
Edukt3-Bromo-1,1-diphenylacetoneHCID 2794635—
Edukt5,5-Dimethyl-1,4,5,6-tetrahydro-pyrimidine-2-thiolHCID 3866487—
LösungsmittelAcetoneHCID 180—
Produkt3-Diphenylmethyl-2,3,6,7-tetrahydro-6,6-dimethyl-5H-thiazolo[3,2-a]pyrimidin-3-ol hydrobromideHCID 15571212—

Reaktionsschritte

A 2.1 g. portion of 1,1-diphenyl-2-propanone is converted to 1-bromo-3,3-diphenyl-2-propanone as described in Example 22. This 1-bromo-3,3-diphenyl-2-propanone is dissolved in 15 ml. of acetone and added to a boiling mixture of 1.0 g. of tetrahydro-5,5-dimethyl-2(1H)-pyrimidinethione in 50 ml. of acetone. The mixture is allowed to stand at room temperature for 24 hours and the resulting solid is collected by filtration, giving the desired product, m.p. 259°-261° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04393004
Quelldatensatzuspto-grants-1983_07
ORD IDord-3130c19ef8eb4df6a7981fdcec590ce9
Quellennotizuspto-grants-1983_07