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Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → tert-Butyl 3-(2-methoxy-2-oxoethylidene)azetidine-1-carboxylate

HRID 1175133
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HRID 1175133 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:11][C:10](=O)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:13][O:14][C:15]([CH:17]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:16]>C1(C)C=CC=CC=1>[C:1]([O:5][C:6]([N:8]1[CH2:11][C:10](=[CH:17][C:15]([O:14][CH3:13])=[O:16])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 17453Acetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 15194043-Oxo-azetidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 56923823tert-Butyl 3-(2-methoxy-2-oxoethylidene)azetidine-1-carboxylate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester (1.67 g; 9.7 mmol) and methoxycarbonyl-methylene-triphenylphosphorane (3.42 g; 10.25 mmol) are dissolved in toluene (5 ml), refluxed for 2.5 hours and left over night at room temperature. The precipitate is filtered off, washed with TBME, and the filtrate purified via chromatography (TBME/hexane 2:8>3:7) to yield the title compound as colorless crystals. 1H-NMR (400 MHz; DMSO-d6): 5.90 (m, 1H); 4.71 (bs, 2H); 4.58 (bs, 2H); 3.67 (s, 3H); 1.42 (s, 9H). MS (m/z) ES+: 171 (10; MH+ minus tert-butyl); 57 (100).

후처리

  1. temperaturerefluxed for 2.5 hours
  2. waitleft over night at room temperature
  3. filtrationThe precipitate is filtered off
  4. washwashed with TBME
  5. customthe filtrate purified via chromatography (TBME/hexane 2:8>3:7)

출처 및 근거

ORD 기록
ord-10c613c2f30549a79f09f1435e1b9d38
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07838674B2

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