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Hydroxylamine → 3,4-Dichlorobenzylthioaceto-hydroxamic acid

HRID 28171
ノート
印刷プレビュー

反応式

HRID 28171 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[Cl:13])[CH2:5][CH2:6][C:7](O)=[S:8].OS(O)(=O)=O.ClC(Cl)C.[NH2:23][OH:24].C[O-].[Na+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[Cl:13])[CH2:5][CH2:6][C:7]([NH:23][OH:24])=[S:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 787HydroxylamineHCID 1118Sulfuric AcidHCID 63651,1-DichloroethaneHCID 10942334Sodium MethoxideHCID 178526174HCID 178526174、化合物

生成物 1

HCID 867361013,4-Dichlorobenzylthioaceto-hydroxamic acid収率 75%

試薬・触媒・溶媒 1

HCID 887
Methanol
溶媒
2 回

実験手順

20.2 g (0.08 mol) of 3,4-dichlorobenzylthioacetic acid are esterified with 10 ml of methanol, 0.6 ml of concentrated H2SO4 and 100 ml of dichloroethane. The mixture is heated under reflux for 4 hours, washed with water and with dilute bicarbonate solution, and dried. The mixture is evaporated in vacuo. The oily residue, in methanol, is treated with a solution of hydroxylamine (0.1 mol) in the presence of 0.18 mol of sodium methylate. After leaving the reactants in contact overnight, the mixture is evaporated to dryness in vacuo, the residue is taken up in water, the mixture is filtered over charcoal and the filtrate is precipitated with 3N HCl, the product is extracted with ether, the extract is dried and evaporated and the product is crystallised in diisopropyl ether. 15 g of the stated product are obtained (yield 71%). Melting point: 75°-76° C.

後処理

  1. temperatureThe mixture is heated
  2. temperatureunder reflux for 4 hours
  3. washwashed with water and with dilute bicarbonate solution
  4. customdried
  5. customThe mixture is evaporated in vacuo
  6. customAfter leaving the reactants in contact overnight
  7. customthe mixture is evaporated to dryness in vacuo
  8. filtrationthe mixture is filtered over charcoal
  9. customthe filtrate is precipitated with 3N HCl
  10. extractionthe product is extracted with ether
  11. customthe extract is dried
  12. customevaporated
  13. customthe product is crystallised in diisopropyl ether

出典と根拠

ORDレコード
ord-a0204dc1ec8643429653b00bdfa853c5
出典データセット
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04225617

反応ノート

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