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

Ethylene Glycol → HCID 3525985, 화합물

HRID 1748315
노트
인쇄 미리보기

반응식

HRID 1748315 반응식
[O:1]=[C:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[CH2:3][C:4]#[N:5].CC1C=CC(S(O)(=O)=O)=CC=1.[CH2:23](O)[CH2:24][OH:25]>C1(C)C=CC=CC=1>[C:6]1([C:2]2([CH2:3][C:4]#[N:5])[O:25][CH2:24][CH2:23][O:1]2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 64799Benzoylacetonitrile

생성물 1

HCID 3525985HCID 3525985, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
150 °C

실험 절차

To a solution of 3-oxo-3-phenylpropanenitrile (10 g, 68.8 mmol) and PTSA (0.027 g, 1.37 mmol) in toluene (120 mL) is added ethylene glycol (120 mL, 2057 mmol). The mixture is heated at 150° C. for 14 h. The solvent is evaporated under reduced pressure and the residue is washed with 10% NaOH solution. The aqueous layer is extracted with diethyl ether (2×100 mL) and the combined organic layers are dried (Na2SO4) and evaporated to provide the crude compound. The crude material is purified over neutral alumina eluting with 1% of ethyl acetate/hexane to afford the title compound as an off white solid (10 g, 77%).

후처리

  1. customThe solvent is evaporated under reduced pressure
  2. washthe residue is washed with 10% NaOH solution
  3. extractionThe aqueous layer is extracted with diethyl ether (2×100 mL)
  4. dry with materialthe combined organic layers are dried (Na2SO4)
  5. customevaporated
  6. customto provide the crude compound
  7. customThe crude material is purified over neutral alumina eluting with 1% of ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-7f77df4e2f994d2c9d98ca73bd8c3592
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150577B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트