홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Water → 4-n-butylthio-benzonitrile

HRID 394849
노트
인쇄 미리보기

반응식

HRID 394849 반응식
Cl[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:16]([SH:20])[CH2:17][CH2:18][CH3:19].O>CC(N(C)C)=O>[CH2:16]([S:20][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1)[CH2:17][CH2:18][CH3:19]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8012ButanethiolHCID 11430Potassium CarbonateHCID 121634-Chlorobenzonitrile

생성물 1

HCID 110196724-n-butylthio-benzonitrile

시약·촉매·용매 1

HCID 31374Dimethylacetamide용매2회

반응 조건

온도
80 °C

실험 절차

To a well-stirred suspension of 41.27 g (0.3 mol) of 4-chlorobenzonitrile, 58.05 g (0.42 mol) of potassium carbonate and 200 ml DMA a solution of 27.06 g (0.3 mol) of 1-butanethiol in 50 ml of DMA are added under an atmosphere of nitrogen. The resulting mixture is heated to 80° C. and stirred at this temperature for 24 hours. Then, the reaction mixture is cooled to room temperature and poured into 750 ml of water. The crude product is extracted with 300 ml of ethyl acetate, washed with water, dried over MgSO4. Thereafter, ethyl acetate is removed. Then, fractional distillation yields 52.88 9 (80.4%) of colorless liquid 4-n-butylthio-benzonitrile.

후처리

  1. additionare added under an atmosphere of nitrogen
  2. temperatureThen, the reaction mixture is cooled to room temperature
  3. extractionThe crude product is extracted with 300 ml of ethyl acetate
  4. washwashed with water
  5. dry with materialdried over MgSO4
  6. customThereafter, ethyl acetate is removed
  7. distillationThen, fractional distillation

출처 및 근거

ORD 기록
ord-d9f3e3f65d3948caaf50f5962f521157
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06603020B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트