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Ethoxalyl chloride → 1-Ethyl-1-ethoxalyl-thiosemicarbazide

HRID 1660325
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HRID 1660325 반응식
[C:1](Cl)([C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:2].[CH2:9]([NH:11][NH:12][C:13]([NH2:15])=[S:14])[CH3:10]>CC(C)=O>[CH2:9]([N:11]([C:1]([C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:2])[NH:12][C:13]([NH2:15])=[S:14])[CH3:10]
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참가 물질

4

반응물 2

HCID 20884Ethoxalyl chlorideHCID 221050282-Ethylhydrazinecarbothioamide

생성물 1

HCID 205581251-Ethyl-1-ethoxalyl-thiosemicarbazide

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Ethoxalyl chloride (10.6 cc) is added dropwise, in the course of 10 minutes, to a solution, at 20° C., of 1-ethyl-thiosemicarbazide (11.9 g) in acetone (200 cc). The temperature rises to 43° C., the mixture is stirred for 1 hour without heating and is concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa), the residue is taken up in methanol (30 cc) and the crystallisation is started. After filtration and drying, 1-ethyl-1-ethoxalyl-thiosemicarbazide (13.2 g) is obtained in the form of a white solid melting at 170° C.

후처리

  1. customrises to 43° C.
  2. temperaturewithout heating
  3. concentrationis concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa)
  4. customthe crystallisation
  5. filtrationAfter filtration
  6. customdrying

출처 및 근거

ORD 기록
ord-c40b265242454c35a03a82b06c881f90
출처 데이터셋
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04307116

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