Reaktionsgleichung
[C:1]([OH:13])(=[O:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]#[CH:11].[Br:14][O-].[Na+].Br[O-].BrBr.OS(O)(=O)=O>[OH-].[Na+]>[Br:14][C:11]#[C:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:1]([OH:13])=[O:12]Komponenten
7
Edukt 5
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 36.45 g (200 mmol) of 10-undecynoic acid in 200 ml 1 N NaOH at 0° C. was added a solution of alkaline sodium hypobromite dropwise over 30 minutes, maintaining the temperature below 5° C. (the hypobromite solution was prepared by the dropwise addition of 35.16 g (220 mmol) of bromine to 55 ml of 20 N NaOH at 0°-5° C.). The mixture was stirred four hours at 0°-5° C., and was then acidified to PH 1 with 9 M H2SO4. The solution was extracted with three 150 ml portions of ether. The combined extracts were dried (Na2SO4) and evaporated yielding 50.159 (96% crude) of a pale yellow solid. THis was used without further purification.
Aufarbeitung
- extractionThe solution was extracted with three 150 ml portions of ether
- dry with materialThe combined extracts were dried (Na2SO4)
- customevaporated
- customyielding 50.159 (96% crude) of a pale yellow solid
- customTHis was used without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-8651c3f7979f4deea05b1bb0ea1e24ce
- Quelldatensatz
- uspto-grants-1984_02
- Patentnummer
- US04431263
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