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Benzyl chloroformate → Benzyl 3-(1,3,4-oxadiazol-2-yl)phenylcarbamate

HRID 1909455
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HRID 1909455 반응식
[O:1]1[CH:5]=[N:4][N:3]=[C:2]1[C:6]1[CH:7]=[C:8]([CH:10]=[CH:11][CH:12]=1)[NH2:9].C(=O)(O)[O-].[Na+].CC(C)=O.O.[CH2:23]([O:30][C:31](Cl)=[O:32])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>O>[CH2:23]([O:30][C:31](=[O:32])[NH:9][C:8]1[CH:10]=[CH:11][CH:12]=[C:6]([C:2]2[O:1][CH:5]=[N:4][N:3]=2)[CH:7]=1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1
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참가 물질

6

반응물 4

HCID 10387Benzyl chloroformateHCID 516892Sodium BicarbonateHCID 162280973-(1,3,4-Oxadiazol-2-yl)anilineHCID 18366337Propan-2-one--water (1/1)

생성물 1

HCID 66851996Benzyl 3-(1,3,4-oxadiazol-2-yl)phenylcarbamate수율 93%

시약·촉매·용매 1

HCID 962Water
용매

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온도
0 °C

실험 절차

A solution of 3-(1,3,4-oxadiazol-2-yl)aniline (1 g, 6.2 mmol) and sodium bicarbonate (1.1 g, 13 mmol) in a 2:1 mixture of acetone/water (10 mL) was cooled to 0° C. Benzylchloroformate (0.92 mL, 6.5 mmol) was added dropwise over 5 minutes. The reaction mixture was brought to room temperature and stirred for 30 minutes at which point LCMS indicated completion of the reaction. The reaction mixture was diluted with water and filtered on a glass frit to give (3-[1,3,4]Oxadiazol-2-yl-phenyl)-carbamic acid benzyl ester as a white powder (1.7 g, 93%). M+1=296.4

후처리

  1. customwas brought to room temperature
  2. customcompletion of the reaction
  3. filtrationfiltered on a glass frit

출처 및 근거

ORD 기록
ord-ec70acd30ba04d0e885cbc006af69858
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598360B2

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