반응식
[CH3:1][O:2][C:3]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([CH:17]=[O:18])=[C:9]2[C:4]=1[CH:5]=[CH:6][CH:7]=[CH:8]2.[CH3:19]C[O-].[Na+].CCO.ClC1C2C(=CC=CC=2)C(C=O)=C2C=1C=CC=C2>C(Cl)Cl.CCCCCC>[CH2:1]([O:2][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[C:10]([CH:17]=[O:18])=[C:11]2[C:16]=1[CH:15]=[CH:14][CH:13]=[CH:12]2)[CH3:19]참가 물질
6
실험 절차
Using the procedure outlined in 13A, except that NaOEt (Aldrich)/EtOH was used instead of NaOCH3 /CH3OH, 10-chloro-9-anthraldehyde (Aldrich) gave 10-ethoxy-9-anthracenecarbaldehyde mp 88°-90°, (CH2Cl2 /hexane) (C, H).
출처 및 근거
- ORD 기록
- ord-2c6e808804a3410cb68d14e085eb99f3
- 출처 데이터셋
- uspto-grants-1988_01
- 특허 번호
- US04719049
연결된 노트
불러오는 중…