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Sodium Hydroxide → tert-Butyl 3-[(5-oxido-4-(phenylsulphonyl)-1,2,5-oxadiazol-3-yl)-oxy]-propionate

HRID 1013431
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HRID 1013431 반응식
[OH-].[Na+].[C:3]1([S:9]([C:12]2[C:16](S(C3C=CC=CC=3)(=O)=O)=[N:15][O:14][N+:13]=2[O-:26])(=[O:11])=[O:10])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[OH:27][CH2:28][CH2:29][C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31]>C1COCC1>[O-:26][N+:13]1[O:14][N:15]=[C:16]([O:27][CH2:28][CH2:29][C:30]([O:32][C:33]([CH3:36])([CH3:35])[CH3:34])=[O:31])[C:12]=1[S:9]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1)(=[O:10])=[O:11]
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 124054663,4-Di(benzenesulfonyl)-2-oxo-1,2,5lambda~5~-oxadiazoleHCID 16218743tert-Butyl 3-hydroxypropanoate

생성물 1

HCID 86629015tert-Butyl 3-[(5-oxido-4-(phenylsulphonyl)-1,2,5-oxadiazol-3-yl)-oxy]-propionate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Aqueous 50% NaOH solution (6.4 g-80 mmol) is added in the course of 15 minutes to a solution, cooled to 15° C., of 3,4-bis(phenylsulphonyl)-1,2,5-oxadiazole 2-oxide (16 g-44 mmol) and tert-butyl 3-hydroxypropionate (10 g-68 mmol) in 200 ml of anhydrous THF. After stirring for 2 hours, the solvent is removed in vacuo and the residue is taken up in 100 ml of water and 100 ml of ethyl acetate. The organic phase is decanted off, washed with saturated NaCl solution, dried with sodium sulphate and evaporated.

후처리

  1. customthe solvent is removed in vacuo
  2. customThe organic phase is decanted off
  3. washwashed with saturated NaCl solution
  4. dry with materialdried with sodium sulphate
  5. customevaporated

출처 및 근거

ORD 기록
ord-c8286877c4e941c59d563b66449d60d9
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981920B2

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