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Ethanol → Caldaret monohydrate

HRID 1066715
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HRID 1066715 반응식
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)=[C:6]([S:8]([OH:11])(=[O:10])=[O:9])[CH:7]=1.C(O)C>O>[OH2:9].[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)=[C:6]([S:8]([OH:11])(=[O:9])=[O:10])[CH:7]=1
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참가 물질

4

반응물 2

HCID 702EthanolHCID 6433076Caldaret

생성물 1

HCID 9816981Caldaret monohydrate수율 177.3%

시약·촉매·용매 1

HCID 962Water용매

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온도
5 °C

실험 절차

The anhydrous crystal of 5-Methyl-2-(1-piperazinyl)-benzenesulfonic acid (10.00 g) and ethanol containing 50% (V/V) water (80 ml) were added in a 200 ml round-bottomed flask and the crystals were thoroughly dissolved by heating under reflux with stirring. The solution was then cooled to 5° C. with stirring and stirring was further continued for 2 hours at the same temperature. The precipitated crystals were collected by suction filtration and washed with ethanol containing 50% (V/V) water (20 ml). The crystals obtained were dried at 50° C. under 90 mmHg for 3 hours to give 5-methyl-2-(1-piperazinyl)benzenesulfonic acid monohydrate as white crystals (9.49 g, yield: 88.7%). After drying was further continued for 27 hours under the same conditions, the weight and the appearance of the monohydrate were not changed. Water content measured by a Karl Fischer water content meter was 6.74%, which further verified that the product was the monohydrate.

후처리

  1. dissolutionthe crystals were thoroughly dissolved
  2. temperatureby heating
  3. temperatureunder reflux
  4. stirringwith stirring
  5. stirringstirring
  6. filtrationThe precipitated crystals were collected by suction filtration
  7. washwashed with ethanol containing 50% (V/V) water (20 ml)
  8. customThe crystals obtained
  9. customwere dried at 50° C. under 90 mmHg for 3 hours

출처 및 근거

ORD 기록
ord-1031e81a87be4b7f9076ca38f6c9ce06
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06245767B1

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