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

Diisobutylaluminumhydride → 2-(2-Bromo-4-fluorophenoxy)propionaldehyde

HRID 1815799
노트
인쇄 미리보기

반응식

HRID 1815799 반응식
[Br:1][C:2]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[C:6](OCC)=[O:7].[H-].C([Al+]CC(C)C)C(C)C>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:3]=1[O:4][CH:5]([CH3:11])[CH:6]=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21225700DiisobutylaluminumhydrideHCID 22144730Ethyl 2-(2'-bromo-4'-fluorophenoxy)propionate

생성물 1

HCID 221447442-(2-Bromo-4-fluorophenoxy)propionaldehyde수율 102.6%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
-78 °C

실험 절차

A solution of 19.4 gm (66.7 mMol) ethyl 2-(2-bromo-4-fluorophenoxy)propionate in 400 mL toluene was cooled to −78° C. at which point 100 mL (100 mMol) diisobutylaluminum hydride (1 M in toluene) were added dropwise over 35 minutes. The reaction mixture was stirred at −78° C. for an additional 20 minutes after the addition was complete and then the reaction was quenched by the addition of methanol. The reaction mixture was warmed to room temperature and then treated with saturated aqueous sodium potassium carbonate. The mixture was stirred for 30 minutes and was then extracted well with ethyl acetate. The organic phases were combined, dried over sodium sulfate, and concentrated under reduced pressure to provide 16.9 gm of crude desired compound.

후처리

  1. additionwere added dropwise over 35 minutes
  2. additionafter the addition
  3. customthe reaction was quenched by the addition of methanol
  4. temperatureThe reaction mixture was warmed to room temperature
  5. additiontreated with saturated aqueous sodium potassium carbonate
  6. stirringThe mixture was stirred for 30 minutes
  7. extractionwas then extracted well with ethyl acetate
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-a35e1f64a7dd427d81486f48e2c5e2fa
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06881733B1

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트