Dicyclohexylcarbodiimide → 4-Benzyloxy-2-chloro-benzoic acid 4-(4-pentyl-phenoxycarbonyl)-phenyl ester
반응식
[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([OH:15])=[O:14])=[C:11]([Cl:18])[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:19]([C:24]1[CH:29]=[CH:28][C:27]([O:30][C:31](=[O:39])[C:32]2[CH:37]=[CH:36][C:35](O)=[CH:34][CH:33]=2)=[CH:26][CH:25]=1)[CH2:20][CH2:21][CH2:22][CH3:23].C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C1C=CN=CC=1.C(Cl)Cl>[CH2:19]([C:24]1[CH:29]=[CH:28][C:27]([O:30][C:31]([C:32]2[CH:37]=[CH:36][C:35]([O:14][C:13](=[O:15])[C:12]3[CH:16]=[CH:17][C:9]([O:8][CH2:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)=[CH:10][C:11]=3[Cl:18])=[CH:34][CH:33]=2)=[O:39])=[CH:26][CH:25]=1)[CH2:20][CH2:21][CH2:22][CH3:23]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
1.84 g (7.0 mmol) of 4-benzyloxy-2-chloro-benzoic acid, 1.90 g (6.7 mmol) of 4-hydroxy-benzoic acid 4-pentyl-phenyl ester and 0.082 g (0.67 mmol) of 4-dimethylaminopyridine were dissolved in 50 mL of methylene chloride followed by the addition of 1.45 g (7.0 mmol) of dicyclohexylcarbodiimide while stirring in the presence of argon. After stirring for 8 hours in the presence of argon, the reaction mixture was filtered and the filtrate was concentrated. The residue was purified by silica gel column chromatography to obtain 3.3 g of a white solid.
후처리
- stirringAfter stirring for 8 hours in the presence of argon
- filtrationthe reaction mixture was filtered
- concentrationthe filtrate was concentrated
- customThe residue was purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-592a9dcd06bb4e2fba91a1c215a09ca2
- 출처 데이터셋
- uspto-grants-2010_02
- 특허 번호
- US07658979B2
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