Phenanthro[1,2-b]furan-2-methanol → Phenanthro[1,2-b]thiophene-2-methanol

HRID 1722548노트

반응식

HRID 1722548 반응식
C1C2C=CC3C4C=CC=CC=4C=CC=3C=2OC=1CO.[CH:20]1[C:21]2[CH:41]=[CH:40][C:39]3[C:38]4[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=4[CH:32]=[CH:31][C:30]=3[C:22]=2[S:23][C:24]=1[C:25](OCC)=[O:26]>C(Cl)Cl.CCCCCC>[CH:20]1[C:21]2[CH:41]=[CH:40][C:39]3[C:38]4[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=4[CH:32]=[CH:31][C:30]=3[C:22]=2[S:23][C:24]=1[CH2:25][OH:26]

참가 물질

4

실험 절차

Using the procedure outlined in 14A, ethyl phenanthro[1,2-b]thiophene-2-carboxylate (H. G. Pars Pharmaceutical Laboratories, Inc.) gave a 98.0% yield of phenanthro[1,2-b]thiophene-2-methanol, mp 169°-170.5° (C,H,S), (CH2Cl2 /hexane).

출처 및 근거

ORD 기록
ord-2039e7cae5e644a18ff551ce64db4f17
출처 데이터셋
uspto-grants-1989_08
특허 번호
US04855453

반응 노트

불러오는 중…