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Water → 2-Amino-1-(3-methoxycarbonyl-2-thioureido)-4-thiocyanatobenzene

HRID 258766
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HRID 258766 반응식
[CH3:1][O:2][C:3]([NH:5][C:6](=[S:20])[NH:7][C:8]1[CH:13]=[CH:12][C:11]([S:14][C:15]#[N:16])=[CH:10][C:9]=1[N+:17]([O-])=O)=[O:4].O>CO>[NH2:17][C:9]1[CH:10]=[C:11]([S:14][C:15]#[N:16])[CH:12]=[CH:13][C:8]=1[NH:7][C:6]([NH:5][C:3]([O:2][CH3:1])=[O:4])=[S:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 203710751-(3-Methoxycarbonyl-2-thioureido)-2-nitro-4-thiocyanatobenzene

생성물 1

HCID 214266632-Amino-1-(3-methoxycarbonyl-2-thioureido)-4-thiocyanatobenzene수율 26.6%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A stirred mixture of 1-(3-methoxycarbonyl-2-thioureido)-2-nitro-4-thiocyanatobenzene (27.0 g.), ferrous chloride tetrahydrate (5.85 g.), methanol (450 ml.) and water (100 ml.) was brought to reflux and treated with reduced iron powder (29.7 g.) portionwise during 5 minutes. The mixture was heated at reflux for one hour, methanol (250 ml.) was added, and the boiling solution was filtered hot. The filtrate was evaporated to dryness and the residue was extracted with boiling methanol (3× 500 ml.). The extract was evaporated and the residue was recrystalised from methyl ethyl ketone (removing some undissolved material by filtration of the hot solution) to give 2-amino-1-(3-methoxycarbonyl-2-thioureido)-4-thiocyanatobenzene (6.5 g.), m.p. 174°-176° C. (with decomposition).

후처리

  1. temperatureto reflux
  2. temperatureThe mixture was heated
  3. temperatureat reflux for one hour
  4. filtrationthe boiling solution was filtered hot
  5. customThe filtrate was evaporated to dryness
  6. extractionthe residue was extracted with boiling methanol (3× 500 ml.)
  7. customThe extract was evaporated
  8. customthe residue was recrystalised from methyl ethyl ketone (
  9. customremoving some undissolved material
  10. filtrationby filtration of the hot solution)

출처 및 근거

ORD 기록
ord-51f4a7ac62334b0eabf12baa0bfa279d
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04034107

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