Allyl Alcohol → [3-(4-Bromophenyl)-4,5-dihydro-1,2-oxazol-5-yl]methanol
Reaktionsgleichung
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([CH:6]=[N:7][OH:8])=[CH:4][CH:3]=1.[CH2:11]([OH:14])[CH:12]=[CH2:13]>O1CCCC1>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]2[CH2:13][CH:12]([CH2:11][OH:14])[O:8][N:7]=2)=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
4-Bromo-benzaldehyde oxime (162 g, 789.9 mmol) and allyl alcohol (130.5 ml) were added to tetrahydrofuran (1000 ml) and then bleach (5305 ml) was added. The reaction was cooled to 0° C. and stirred for 3 hrs. The precipitate was collected and washed with water (2×300 ml) to give the desired product (137 g).
Aufarbeitung
- additionwas added
- customThe precipitate was collected
- washwashed with water (2×300 ml)
Quellen und Nachweise
- ORD-Eintrag
- ord-e016b6fdce5d44569339c050c2dfa5ea
- Quelldatensatz
- uspto-grants-2008_07
- Patentnummer
- US07396847B2
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