Reaktionsgleichung
[C:1]([OH:20])(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C:21]1(O)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.P(=O)(O)(O)[OH:29]>>[OH:29][C:2]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:1]([OH:20])=[O:19]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 200 °C
Versuchsvorschrift
A 500-ml autoclave was charged with 166 g of commercial oleic acid (product of Nippon Oils & Fats Co., Ltd.), 169 g of phenol (product of Katayama Kagaku Kogyo K.K.), 6.6 g of activated clay (Nippon Kassei Hakudo K.K.), and 0.13 g of 85% aqueous phosphoric acid (product of Katayama Kagaku Kogyo K.K.). After purging the autoclave with nitrogen gas, the contents were allowed to react by heating at 200° C. for 4 hours. After completion of the reaction, the activated clay was filtered off and the unreacted phenol was distilled away at 80°-100° C., 3 mmHg to yield a yellow viscous reaction product in an amount of 224 g.
Aufarbeitung
- customAfter purging the autoclave with nitrogen gas
- customto react
- customAfter completion of the reaction
- filtrationthe activated clay was filtered off
- distillationthe unreacted phenol was distilled away at 80°-100° C.
- custom3 mmHg to yield a yellow viscous reaction product in an amount of 224 g
Quellen und Nachweise
- ORD-Eintrag
- ord-c1c552b8069745d8a6d1ddec01b86e24
- Quelldatensatz
- uspto-grants-1989_12
- Patentnummer
- US04888132
Verknüpfte Notizen
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