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Phosphorus oxychloride → (E)-Methyl 11-chlorodibenzo[b,f][1,4]oxazepine-8-carboxylate

HRID 1907777
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인쇄 미리보기

반응식

HRID 1907777 반응식
O=[C:2]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][C:5]2[CH:13]=[CH:14][C:15]([C:17]([O:19][CH3:20])=[O:18])=[CH:16][C:4]=2[NH:3]1.O=P(Cl)(Cl)[Cl:23]>>[Cl:23][C:2]1=[N:3][C:4]2[CH:16]=[C:15]([C:17]([O:19][CH3:20])=[O:18])[CH:14]=[CH:13][C:5]=2[O:6][C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]1=2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 59737222Methyl 11-oxo-10,11-dihydrodibenzo[b,f][1,4]oxazepine-8-carboxylate

생성물 1

HCID 58875660(E)-Methyl 11-chlorodibenzo[b,f][1,4]oxazepine-8-carboxylate수율 100%

반응 조건

온도
100 °C

실험 절차

Compound 548 (1.00 g, 3.71 mmol)) was suspended in POCl3 (20 mL). The reaction mixture was stirred at 100° C. for 3 h. POCl3 was removed on rotovap. The crude product was dissolved in ethyl acetate and washed with 2M Na2CO3 solution then with NaHCO3 saturated solution and finally with brine. The organic layer was separated and dried with Na2SO4, filtered and concentrated via rotary evaporation to afford compound 549 (1.069 g, 100%) as a orange solid that was taken on without further purification.

후처리

  1. customPOCl3 was removed on rotovap
  2. dissolutionThe crude product was dissolved in ethyl acetate
  3. washwashed with 2M Na2CO3 solution
  4. customThe organic layer was separated
  5. dry with materialdried with Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated via rotary evaporation

출처 및 근거

ORD 기록
ord-185d9d493deb44baac8f63ab34c284a5
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598168B2

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