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

Acetone → 3-Buten-2-one,4-(4-fluorophenyl)-

HRID 1189569
노트
인쇄 미리보기

반응식

HRID 1189569 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[CH3:10][C:11](=[O:13])[CH3:12].[OH-].[Na+]>O>[F:1][C:2]1[CH:9]=[CH:8][C:5](/[CH:6]=[CH:10]/[C:11](=[O:13])[CH3:12])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180AcetoneHCID 14798Sodium HydroxideHCID 680234-Fluorobenzaldehyde

생성물 1

HCID 57028883-Buten-2-one,4-(4-fluorophenyl)-수율 100%

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
65 °C

실험 절차

To a mixture of 4-fluorobenzaldehyde (5 mL, 45.2 mmol), propan-2-one (9.13 mL, 124 mmol), and water (9.5 mL) was added 12 mL of a 1% solution of NaOH in water. The reaction mixture was heated at 65° C. for 2 h. The mixture was then partitioned between EtOAc and ice water, the organic layer separated and the aqueous layer was extracted twice with EtOAc. The combined organic layers were dried with MgSO4 and concentrated under vacuum. The product was obtained as a yellow oil and was used in the next step without further purification (7.93 g, 48.3 mmol, 100% yield). 1H NMR (400 MHz, CDCl3) δ (ppm) 7.54-7.51 (m, 2H), 7.47 (d, 1H), 7.08 (t, 2H), 6.64 (d, 1H), 2.37 (s, 3H).

후처리

  1. customThe mixture was then partitioned between EtOAc and ice water
  2. customthe organic layer separated
  3. extractionthe aqueous layer was extracted twice with EtOAc
  4. dry with materialThe combined organic layers were dried with MgSO4
  5. concentrationconcentrated under vacuum
  6. customThe product was obtained as a yellow oil
  7. customwas used in the next step without further purification (7.93 g, 48.3 mmol, 100% yield)

출처 및 근거

ORD 기록
ord-626102335e8a47ad8ab0d9002fc4737b
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08674115B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트