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

Water → (E)-1-Chloro-2-propenylbenzene

HRID 537383
노트
인쇄 미리보기

반응식

HRID 537383 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]=O.[CH3:10][CH2:11]C(=O)CC.B(F)(F)F.CCOCC.O>CCCCCC>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1/[CH:8]=[CH:10]/[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 69962-ChlorobenzaldehydeHCID 7288Ethyl ketoneHCID 8000Boron trifluoride etherate

생성물 1

HCID 14419677(E)-1-Chloro-2-propenylbenzene수율 59.3%

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

48 ml of 2-chlorobenzenaldehyde (0.42 mol) and 49.7 ml of 3-pentanone (0.47 mol) were dissolved in 600 mL of hexane in flask, and then stirred with raising the temperature. 53.6 ml of Boron trifluoride etherate (BF3OEt2, 0.42 mol) was added to the resultant under reflux conditions. When the reaction was completed, water was added thereto. After layer separation, the obtained organic layer was washed twice with 1M sodium hydroxide solution (1M NaOH), and then the separated organic layer was washed with water. The separated organic layer was dehydrated with anhydrous magnesium sulfate (MgSO4) and concentrated. The concentrated residue was purified by a silica gel column chromatography to produce the title compound (38 g, yield 58%). 1H NMR (400 MHz, CDCl3) δ1.94 (d, J=4.8 Hz, 3H), 6.24 (m, 1H), 6.78 (d, J=14 Hz, 1H), 7.11˜7.51 (m, 4H)

후처리

  1. temperaturewith raising the temperature
  2. customAfter layer separation
  3. washthe obtained organic layer was washed twice with 1M sodium hydroxide solution (1M NaOH)
  4. washthe separated organic layer was washed with water
  5. concentrationconcentrated
  6. customThe concentrated residue was purified by a silica gel column chromatography

출처 및 근거

ORD 기록
ord-6da739ff5af1461286a9065e89f4ca77
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859817B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트