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2-Aminothiazole → 2-(1H-pyrrol-1-yl)-1,3-thiazole

HRID 1576278
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반응식

HRID 1576278 반응식
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N:6]=1.[CH3:7][CH:8]1[CH2:12][CH2:11]C(C)O1.[OH-].[Na+]>C(O)(=O)C>[S:3]1[CH:4]=[CH:5][N:6]=[C:2]1[N:1]1[CH:11]=[CH:12][CH:8]=[CH:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 21552-AminothiazoleHCID 138552,5-DimethyltetrahydrofuranHCID 14798Sodium Hydroxide

생성물 1

HCID 2986802-(1H-pyrrol-1-yl)-1,3-thiazole

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 55.5 g (0.5 mole) 2-aminothiazole (90% pure) and 66 g (0.5 mole) 2,5-dimethyltetrahydrofuran is placed in a 1-liter 3-neck flask equipped with a stirrer, addition funnel, thermometer, and condenser, and 200 ml glacial acetic acid is added dropwise with stirring while maintaining the temperature below 20°C. After stirring for an additional 15 minutes, the reaction mixture is refluxed for 30 minutes and then cooled, made basic (pH 9-10) with 375 ml 30% sodium hydroxide, and steam-distilled to yield 1500 ml distillate.

후처리

  1. customis placed in a 1-liter 3-neck flask
  2. customequipped with a stirrer, addition funnel
  3. temperaturewhile maintaining the temperature below 20°C
  4. stirringAfter stirring for an additional 15 minutes
  5. temperaturethe reaction mixture is refluxed for 30 minutes
  6. temperaturecooled
  7. distillationsteam-distilled
  8. customto yield 1500 ml distillate

출처 및 근거

ORD 기록
ord-a913f47527dd42d68ca9df402916385f
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03980089

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