반응식
N#N.[CH3:3][O:4][C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][CH:9]=[C:10]([O:15][CH3:16])[CH:11]=2)[CH:6]=1.[N:17]1([CH2:23][CH2:24][O:25][C:26]2[CH:34]=[CH:33][C:29]([C:30](Cl)=[O:31])=[CH:28][CH:27]=2)[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1.[Cl-].[Al+3].[Cl-].[Cl-]>C(Cl)Cl.O>[CH3:16][O:15][C:10]1[CH:9]=[CH:8][C:7]2[C:12](=[CH:13][CH:14]=[C:5]([O:4][CH3:3])[CH:6]=2)[C:11]=1[C:30]([C:29]1[CH:28]=[CH:27][C:26]([O:25][CH2:24][CH2:23][N:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[CH:34][CH:33]=1)=[O:31]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 0 °C
실험 절차
In a dry round bottom flask equipped with stir bar, temperature probe and N2 line, dissolve 2,6-dimethoxynaphthalene (1.0 eq) in CH2Cl2 (5 volume equivalents) at ambient temperature. Cool the solution to 0° C. in with an ice bath, and add 4-(2-piperidin-1-yl-ethoxy)-benzoyl chloride (1.1 eq). Add aluminum chloride (2.0 eq). Once the reaction is determined to be complete, quench the reaction slowly with 1 N NaOH and dilute with additional water and CH2Cl2. Wash the aqueous layer with (1×20 mL) of CH2Cl2. Combine the organic extracts and wash with brine and dry (Na2SO4). Recrystallize the crude product from methanol to give (2,6-dimethoxy-naphthalen-1-yl)[4(2-piperidin-1-yl-ethoxy)-phenyl]-methanone (average yield 68%).
후처리
- customIn a dry round bottom flask equipped
- customquench
- customthe reaction slowly with 1 N NaOH
- washWash the aqueous layer with (1×20 mL) of CH2Cl2
- washwash with brine
- dry with materialdry (Na2SO4)
- customRecrystallize the crude product from methanol
출처 및 근거
- ORD 기록
- ord-3d8ec612189a4600be88781b87d7df3d
- 출처 데이터셋
- uspto-grants-2007_09
- 특허 번호
- US07271264B2
연결된 노트
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