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Water → HCID 12097381, 화합물

HRID 989468
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HRID 989468 반응식
O.C(=O)([O-])[O-].[K+].[K+].S(O[CH2:13][C:14]([NH2:17])([CH3:16])[CH3:15])(O)(=O)=O.[CH2:18]([SH:26])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]>C(O)C>[CH3:15][C:14]([NH2:17])([CH3:16])[CH2:13][S:26][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]
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참가 물질

6

반응물 4

HCID 962WaterHCID 81441-OctanethiolHCID 11430Potassium CarbonateHCID 2928692-Amino-2-methyl-1-propanol hydrogen sulfate

생성물 1

HCID 12097381HCID 12097381, 화합물수율 100%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

In a mixed solvent of 10 ml of water and 10 ml of ethanol was suspended 1.38 g (10 mmol) of potassium carbonate. To the suspension were added 0.85 g (5 mmol) of 2-amino-2-methylpropyl hydrogensulfate and 0.73 g (5 mmol) of 1-octanethiol, and the resulting mixture was gently refluxed for 8 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and the desired compound was extracted three times with ethyl acetate. The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and then distilled under reduced pressure to remove the solvent, whereby 1.08 g of 2-methyl-1-n-octylthio-2-propylamine was obtained. The purity was measured in terms of area percentage by gas chromatography and found to be 91%.

후처리

  1. temperaturethe resulting mixture was gently refluxed for 8 hours
  2. customAfter completion of the reaction
  3. extractionthe desired compound was extracted three times with ethyl acetate
  4. washThe combined organic layer was washed with saturated aqueous sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationdistilled under reduced pressure
  7. customto remove the solvent

출처 및 근거

ORD 기록
ord-4b50b85bcdb649c2860d9ebdf3a816df
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06639109B1

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