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

(3-Isopropenyl-4-methoxyphenyl)acetonitrile → 3-Isopropyl-4-methoxyphenylacetonitrile

HRID 2076710
노트
인쇄 미리보기

반응식

HRID 2076710 반응식
[C:1]([C:4]1[CH:5]=[C:6]([CH2:12][C:13]#[N:14])[CH:7]=[CH:8][C:9]=1[O:10][CH3:11])([CH3:3])=[CH2:2]>C(O)C.[C].[Pd]>[CH:1]([C:4]1[CH:5]=[C:6]([CH2:12][C:13]#[N:14])[CH:7]=[CH:8][C:9]=1[O:10][CH3:11])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 67119142(3-Isopropenyl-4-methoxyphenyl)acetonitrile

생성물 1

HCID 109103103-Isopropyl-4-methoxyphenylacetonitrile수율 91.3%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매

실험 절차

(3-Isopropenyl-4-methoxyphenyl)acetonitrile (4.42 g, 23.61 mmol) obtained in Example (109-1) was dissolved in ethanol (50 ml) and 10% palladium-carbon (1 g) was added thereto, and the mixture was stirred at room temperature under a hydrogen atmosphere for 30 minutes. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=4/1) to give (3-isopropyl-4-methoxyphenyl)acetonitrile (4.08 g, yield: 91%).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe residue obtained
  4. customwas purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=4/1)

출처 및 근거

ORD 기록
ord-2a9894b0e50c4b5d83e67b635829ac4b
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07923573B2

반응 노트

불러오는 중…