Benzyl 2-(triphenyl-lambda5-phosphanylidene)acetate → Benzyl (oxetan-3-ylidene)acetate

HRID 1476061노트

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HRID 1476061 반응식
[O:1]1[CH2:4][C:3](=O)[CH2:2]1.C1(P(=[CH:25][C:26]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[O:27])(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>ClCCl>[O:1]1[CH2:2][C:3](=[CH:25][C:26]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[O:27])[CH2:4]1

참가 물질

4

실험 절차

Under argon and at 0° C., 3.0 g (41.63 mmol) of oxetan-3-one (CAS Reg.-No. 6704-31-0) were dissolved in 50 ml of dichloromethane, and 18.8 g (45.79 mmol) of benzyl (triphenyl-λ5-phosphanylidene)acetate were then added. The reaction mixture was then slowly warmed to room temperature and stirred for another 15 minutes. The reaction solution was then concentrated to dryness. The residue was taken up in 25 ml of diethyl ether and stirred, and the mixture was kept at 4° C. for 12 h. The precipitated triphenylphosphine oxide was filtered off and the filtrate was concentrated to dryness. The crude product obtained was purified chromatographically on silica gel (mobile phase cyclohexane/ethyl acetate 4:1→1:1). This gave 4.2 g (20.57 mmol, 49% of theory) of the title compound.

후처리

  1. concentrationThe reaction solution was then concentrated to dryness
  2. stirringstirred
  3. waitthe mixture was kept at 4° C. for 12 h
  4. filtrationThe precipitated triphenylphosphine oxide was filtered off
  5. concentrationthe filtrate was concentrated to dryness

출처 및 근거

ORD 기록
ord-9a897c4ba3364f69a0ede222aebb2be8
출처 데이터셋
uspto-grants-2015_04
특허 번호
US09018414B2

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