Benzaldehyde → 1-Phenylbut-3-en-1-ol

HRID 983765

반응식

HRID 983765 반응식
C([O:5][CH2:6][CH2:7][CH2:8][CH3:9])CCC.C(Br)C=C.C([Mg]Br)(C)C.C(=O)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C(O[Ti](OC(C)C)(OC(C)C)OC(C)C)(C)C.Cl>[C:20]1([CH:6]([OH:5])[CH2:7][CH:8]=[CH2:9])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

참가 물질

7

반응 조건

온도
0 °C

실험 절차

To 0.90 ml (3.0 mmol) of tetraisopropoxytitanium and 5 ml of n-butyl ether solution containing allyl bromide (3.0 mmol) was added dropwise at −78° C. 6.2 ml of 0.97M n-butyl ether solution containing isopropylmagnesium bromide (6.0 mmol). After stirring at −50° C. to −40° C. for 1 hour, the reaction liquid was given 0.21 ml (2.1 mmol) of benzaldehyde and heated to 0° C. over 30 minutes. With 10 ml of 3N hydrochloric acid added, the solution was heated to room temperature and separated into layers. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate. After drying with anhydrous magnesium sulfate, the solution was freed of solvent by vacuum distillation. The residues were purified by silica gel chromatography. Thus there was obtained 252 mg of 1-phenyl-3-buten-1-ol (81% yields based on benzaldehyde).

후처리

  1. additionwas added dropwise at −78° C
  2. customthe reaction liquid
  3. temperaturethe solution was heated to room temperature
  4. customseparated into layers
  5. washThe organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate
  6. dry with materialAfter drying with anhydrous magnesium sulfate
  7. distillationthe solution was freed of solvent by vacuum distillation
  8. customThe residues were purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-011e1e4df19c46d5a267e3777b4ac4ce
출처 데이터셋
uspto-grants-2005_03
특허 번호
US06867161B1

연결된 노트

불러오는 중…