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Sodium Cyanide → 2-(2-(Methylthio)phenyl)acetonitrile

HRID 440542
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HRID 440542 반응식
P(Br)(Br)Br.[CH3:5][S:6][C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH2:9]O.[C-:15]#[N:16].[Na+]>C1(C)C=CC=CC=1.O.C(O)C>[CH3:5][S:6][C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH2:9][C:15]#[N:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 8929Sodium CyanideHCID 24614Phosphorus tribromideHCID 3551404(2-Methylsulfanylphenyl)methanol

생성물 1

HCID 130200632-(2-(Methylthio)phenyl)acetonitrile

시약·촉매·용매 3

HCID 702Ethanol용매HCID 962Water용매2회
HCID 1140
Toluene
용매
2회

반응 조건

온도
40 °C

실험 절차

Phosphorus tribromide (75 g) in toluene (50 ml) was added to a stirred mixture of 2-methylthiobenzyl alcohol (42.5 g) in toluene (25 ml) over 10 minutes at 5° C. The mixture was then stirred at 40° C. for 1 hour, water (100 ml) was added and stirring continued at ambient temperature for 1 hour. The organic layer was separated and the aqueous layer extracted with ethyl acetate. The combined organic layers yielded an oil. The oil (58.6 g) was dissolved in a 1:2 mixture of water and ethanol and sodium cyanide (26.5 g) was added over 15 minutes. The mixture was stirred at 50° C. for 1.5 hours then poured onto water (500 ml) and extracted with ethyl acetate. The extract yielded 2-methylthiophenylacetonitrile.

후처리

  1. stirringstirring
  2. waitcontinued at ambient temperature for 1 hour
  3. customThe organic layer was separated
  4. extractionthe aqueous layer extracted with ethyl acetate
  5. customThe combined organic layers yielded an oil
  6. additionwas added over 15 minutes
  7. stirringThe mixture was stirred at 50° C. for 1.5 hours
  8. additionthen poured onto water (500 ml)
  9. extractionextracted with ethyl acetate

출처 및 근거

ORD 기록
ord-2bbfef484914458e8f84be195ffb7257
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05519034

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