반응식
[NH:1]([C:3](=[O:32])[CH2:4][CH2:5][N:6]1[C:19](=[O:20])[C:9]2([CH2:14][C:13]([CH3:16])([CH3:15])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]2)[O:8][C:7]21[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[NH2:2].[CH3:33][CH:34]1[CH2:44][CH2:43][CH:37]2[C:38]([O:40][C:41](=O)[CH:36]2[CH2:35]1)=[O:39].O.CCCCC>C1(C)C(C)=CC=CC=1>[CH3:33][CH:34]1[CH2:44][CH2:43][CH:37]2[C:38]([N:2]([NH:1][C:3](=[O:32])[CH2:4][CH2:5][N:6]3[C:19](=[O:20])[C:9]4([CH2:14][C:13]([CH3:15])([CH3:16])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]4)[O:8][C:7]43[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31]4)[C:41](=[O:40])[CH:36]2[CH2:35]1)=[O:39]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
The hydrazide of Example 1, 13.5 g (0.03 mole), was added to 225 ml xylene at 75° C. Added dropwise to this was 4-methylhexahydrophthalic anhydride, 5.1 g (0.03 mole) in 25 ml xylene. The apparatus was fitted with a Dean Stark water separation assembly and the reaction mixture was heated to reflux for 4 hours with azeotropic removal of water as it formed. The xylenes were stripped using aspirator vacuum and the residual sticky solid was slurried with 300 ml pentane. The solid was filtered and dried for 2 hours on the filter funnel. The white solid product weighed 11.7 g and had a melting range of 210°-212° C. The infrared spectrum (mull) showed two carbonyl bands at 1690 and 1730 cm-1.
후처리
- temperaturethe reaction mixture was heated
- customformed
- filtrationThe solid was filtered
- customdried for 2 hours on the filter funnel
출처 및 근거
- ORD 기록
- ord-1ce6e273f96b447ca991dee7f0f7384c
- 출처 데이터셋
- uspto-grants-1994_10
- 특허 번호
- US05352719
연결된 노트
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