Reaktionsgleichung
[H-].[Na+].Br[C:4]1[N:9]=[CH:8][CH:7]=[CH:6][N:5]=1.[CH:10]1([CH2:16][OH:17])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1>C1COCC1>[CH:10]1([CH2:16][O:17][C:4]2[N:9]=[CH:8][CH:7]=[CH:6][N:5]=2)[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
NaH (1.1 equivalent) is added to an equimolar mixture of 2-bromopyrimidine and cyclohexylmethanol in THF. The reaction mixture is stirred at +60° C. for 18 hours, cooled to room temperature, partitioned between H2O and ethyl acetate. Organic portion is separated, dried over anhydrous Na2SO4 and concentrated under reduced pressure to give 2-(cyclohexylmethoxy)pyrimidine.
Aufarbeitung
- custompartitioned between H2O and ethyl acetate
- customOrganic portion is separated
- dry with materialdried over anhydrous Na2SO4
- concentrationconcentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-08bcb063c6f745de8323dde4cf803480
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09447078B2
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