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Water → 1-(4-Methylphenyl)isoquinoline-5-acetonitrile

HRID 1156903
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인쇄 미리보기

반응식

HRID 1156903 반응식
[C-:1]#[N:2].[Na+].[CH3:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:20]3[C:15](=[C:16]([CH2:21]Cl)[CH:17]=[CH:18][CH:19]=3)[CH:14]=[CH:13][N:12]=2)=[CH:7][CH:6]=1.O>CS(C)=O>[CH3:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:20]3[CH:19]=[CH:18][CH:17]=[C:16]([CH2:21][C:1]#[N:2])[C:15]=3[CH:14]=[CH:13][N:12]=2)=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 8929Sodium CyanideHCID 12851845HCID 12851845, 화합물

생성물 1

HCID 128518461-(4-Methylphenyl)isoquinoline-5-acetonitrile수율 84.4%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

Sodium cyanide (1.89 g) was dissolved in 100 ml of dimethylsulfoxide, and 8.6 g of 1-(4-methylphenyl)-5-chloromethylisoquinoline was added. At room temperature, the mixture was stirred for 1 hour. After the reaction, the reaction mixture was poured into water, extracted with ether, washed in water, and dried. The solvent was distilled off. The residue was recrystallized from ether to afford 7 g of 1-(4-methylphenyl)isoquinoline-5-acetonitrile as prisms having a melting point of 101.7° to 102.1° C.

후처리

  1. customAfter the reaction
  2. extractionextracted with ether
  3. washwashed in water
  4. customdried
  5. distillationThe solvent was distilled off
  6. customThe residue was recrystallized from ether

출처 및 근거

ORD 기록
ord-58ea6b15981d459aac30441c3d326c73
출처 데이터셋
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04337256

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