反应方程式
CCCC.[C:5]1(C)[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[CH:11]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[C:12]([OH:14])=[O:13].[O:32]=O.C[C:35](CC)=[O:36]>C([O-])(=O)C.[Co+2].C([O-])(=O)C>[C:35]([C:11]([C:6]1[CH:5]=[CH:10][CH:9]=[CH:8][CH:7]=1)([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[C:12]([OH:14])=[O:13])([OH:36])=[O:32]参与物
6
实验过程
The oxidation procedure of Example I was repeated except that only 40 gms cobalt (II) acetate was employed. Also, for this reaction 40 gms methylethyl ketone and 72 gms butane were charged to the reactor. Eighty percent conversion of the tolylstearic acid was achieved after only four hours reaction (105° C. and 350 psig O2). Carboxyphenylstearic acid was obtained in 47.9% yield.
后处理
- additionwere charged to the reactor
来源与证据
- ORD记录
- ord-0445cac1340449bb900981407bee45ad
- 来源数据集
- uspto-grants-1982_10
- 专利号
- US04356315
关联笔记
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