반응식
[CH2:1](S)[CH2:2]C.[C:5]1(=[O:11])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1.[CH2:12](S)[CH2:13][CH2:14][CH3:15].[CH3:17][CH2:18][C:19](=[O:22])[CH2:20][CH3:21]>>[OH:22][C:19]1[CH:20]=[CH:21][C:12]([C:13]([C:8]2[CH:9]=[CH:10][C:5]([OH:11])=[CH:6][CH:7]=2)([CH2:1][CH3:2])[CH2:14][CH3:15])=[CH:17][CH:18]=1참가 물질
5
실험 절차
3,3-Bis(p-hydroxyphenyl)pentane was prepared by repeating the procedure of Example I with the exceptions that 86 grams of 3-pentanone, and 0.5 gram of propanethiol were respectively employed in place of the cyclohexanone and butanethiol. The purity of the resulting above product was 99.5, and it had a melting point of 207° to 208° C. NMR data for this product was as follows:
출처 및 근거
- ORD 기록
- ord-06b0221730954dac940020f013f59220
- 출처 데이터셋
- uspto-grants-1988_08
- 특허 번호
- US04766255
연결된 노트
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