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HCID 21425810, 화합물 → HCID 54056356, 화합물

HRID 258517
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HRID 258517 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[C:9](=[O:14])[CH2:10]S(C)=O.[C:15]([C:17]1[CH:26]=[CH:25][C:20]([CH:21]=[CH:22][CH:23]=O)=[CH:19][CH:18]=1)#[N:16].COC1C2OC(C=CC3C=CC(C#N)=CC=3)=CC(=O)C=2C=CC=1>>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]2[O:1][C:23]([CH:22]=[CH:21][C:20]3[CH:19]=[CH:18][C:17]([C:15]#[N:16])=[CH:26][CH:25]=3)=[CH:10][C:9](=[O:14])[C:3]=2[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 21425810HCID 21425810, 화합물HCID 54065145HCID 54065145, 화합물HCID 54292473HCID 54292473, 화합물

생성물 1

HCID 54056356HCID 54056356, 화합물

실험 절차

This was prepared by reacting 6.36 g of 2'-hydroxy-5'-methyl-2-(methylsulfinyl)acetophenone with 6.36 g of p-cyanocinnamaldehyde in analogous fashion to 4-[2-(8-methoxy-4-oxo-4H-1-benzopyran-2-yl)ethenyl]benzonitrile. The material was recrystallized from toluene, mp 249°-51°; yield 3.5g (41%) λ max mμ (ε) 219 (19,300); 278 (13,500), 339 (41,000); ν max 825 (m), 980 (m), 1235 (m), 1580 (m), 1630 (m), 1670 (s), 2240 (m) cm-1.

후처리

  1. customThis was prepared
  2. customThe material was recrystallized from toluene, mp 249°-51°

출처 및 근거

ORD 기록
ord-82a15110e12a49988ae71f185d3b6d15
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04033845

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