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Trifluoroacetic acid → 2-(2-Hydroxyethyl)-6-nitro-2,3-dihydroimidazo[2,1-b]oxazole

HRID 856166
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HRID 856166 반응식
FC(F)(F)C(O)=O.COC[O:11][CH2:12][CH2:13][CH:14]1[O:18][C:17]2=[N:19][C:20]([N+:22]([O-:24])=[O:23])=[CH:21][N:16]2[CH2:15]1>C(Cl)Cl>[OH:11][CH2:12][CH2:13][CH:14]1[O:18][C:17]2=[N:19][C:20]([N+:22]([O-:24])=[O:23])=[CH:21][N:16]2[CH2:15]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 230815542-(2-Methoxymethoxyethyl)-6-nitro-2,3-dihydroimidazo[2,1-b]oxazole

생성물 1

HCID 230813022-(2-Hydroxyethyl)-6-nitro-2,3-dihydroimidazo[2,1-b]oxazole수율 67.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Trifluoroacetic acid (2 ml) was added to a solution of 2-(2-methoxymethoxyethyl)-6-nitro-2,3-dihydroimidazo[2,1-b]oxazole prepared in Example 25 (0.2 g, 0.822 mmol) in methylene chloride (10 ml) followed by stirring at room temperature overnight. The mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/methanol=100/1), and crystallized from methanol-diisopropyl ether to afford 2-(2-hydroxyethyl)-6-nitro-2,3-dihydroimidazo[2,1-b]oxazole (0.11 g, yield 65%) as a light yellow powder.

후처리

  1. concentrationThe mixture was concentrated under reduced pressure
  2. customthe residue was purified by silica gel column chromatography (methylene chloride/methanol=100/1)
  3. customcrystallized from methanol-diisopropyl ether

출처 및 근거

ORD 기록
ord-6180e0dcca114e6595b814cf8a8c07a5
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262212B2

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