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Octanoyl chloride → HCID 178442555, 화합물

HRID 1171447
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HRID 1171447 반응식
[C:1](Cl)(=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH3:11][NH:12][C:13](=[S:16])[NH:14][NH2:15].[OH-].[K+]>O1CCCC1>[CH2:2]([C:1]1[N:12]([CH3:11])[C:13]([SH:16])=[N:14][N:15]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8124Octanoyl chlorideHCID 14797Potassium HydroxideHCID 2723853N-Methylhydrazinecarbothioamide

생성물 1

HCID 178442555HCID 178442555, 화합물수율 90.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

5 g (30.74 mmol, 1 eq) of octanoyl chloride and 3.58 g (33.81 mmol, 1.1 eq) of 4-methyl-3-thiosemicarbazide in solution in 350 ml of tetrahydrofuran are stirred for 3 hours at room temperature. The solution is concentrated to dryness. The solid obtained is taken up in 350 ml of a 10% aqueous potassium hydroxide solution 35 g (0.82 mmol, 20 eq). The reaction mixture is stirred overnight under reflux. In the cold state, the reaction medium is acidified. The precipitate obtained is filtered, washed with a minimum of water and then dried. 5.94 g (90%) of the expected compound are obtained.

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후처리

  1. concentrationThe solution is concentrated to dryness
  2. customThe solid obtained
  3. temperatureunder reflux
  4. customThe precipitate obtained
  5. filtrationis filtered
  6. washwashed with a minimum of water
  7. customdried

출처 및 근거

ORD 기록
ord-4ccef557b0134e728b4a16cff9905cf2
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07829588B2

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