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Dimethylformamide → 2-(5-methyl-1H-imidazol-4-yl)ethanol oxalate

HRID 49581
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HRID 49581 반응식
Br[CH:2]1[CH2:6][CH2:5][O:4][C:3]1([CH3:8])[OH:7].C(O)(=[O:11])C.[CH:13]([NH2:15])=[NH:14].C(NCC)C.CN(C)[CH:23]=[O:24]>>[C:23]([OH:24])(=[O:11])[C:3]([OH:7])=[O:4].[CH3:8][C:3]1[NH:15][CH:13]=[N:14][C:2]=1[CH2:6][CH2:5][OH:4]
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참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 8021DiethylamineHCID 160693Formamidine acetateHCID 212994013-Bromo-2-methyl-tetrahydrofuran-2-ol

생성물 1

HCID 212994002-(5-methyl-1H-imidazol-4-yl)ethanol oxalate수율 42%

반응 조건

온도
80 °C

실험 절차

5.0 g of 3-bromo-2-methyl-tetrahydrofuran-2-ol and 5.75 g of formamidine acetate were added to 15 ml of N,N-dimethylformamide. 5 g of diethylamine was slowly added to the reaction mixture, which was then stirred for about 4 hours at 80° C. and was distilled in vacuo for about 1 hour at the same temperature. The resulting oily residue was diluted with 25 ml of acetone. 4.95 g of oxalic acid was added to the reaction mixture, which was then stirred for about 1 hour. The resulting solid was filtered and washed with acetone to give 2.5 g of 2-(5-methyl-1H-imidazol-4-yl)ethanol oxalate (yield: 42%).

후처리

  1. distillationwas distilled in vacuo for about 1 hour at the same temperature
  2. additionThe resulting oily residue was diluted with 25 ml of acetone
  3. addition4.95 g of oxalic acid was added to the reaction mixture, which
  4. stirringwas then stirred for about 1 hour
  5. filtrationThe resulting solid was filtered
  6. washwashed with acetone

출처 및 근거

ORD 기록
ord-4f07a90ad4d24bee9af17a0712dbf074
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706888B2

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