Piperidine → 1-[3-(4-Iodophenoxy)propyl]piperidine
반응식
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([I:12])=[CH:8][CH:7]=1.C(=O)([O-])[O-].[K+].[K+].[NH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1>CN(C)C=O>[I:12][C:9]1[CH:10]=[CH:11][C:6]([O:5][CH2:4][CH2:3][CH2:2][N:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)=[CH:7][CH:8]=1참가 물질
5
실험 절차
Following the procedure described in example 1§E, but starting from 1-(3-chloropropoxy)-4-iodobenzene (3 g), potassium carbonate (4.15 g) and piperidine (1.7 g) in N,N-dimethylformamide (30 mL) affords 3.49 g of 1-[3-(4-iodophenoxy)propyl]piperidine used without further purification.
출처 및 근거
- ORD 기록
- ord-41d383dbdb9440319f43c1491c845a91
- 출처 데이터셋
- uspto-grants-2011_12
- 특허 번호
- US08076329B2
반응 노트
불러오는 중…