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Water → 4-Nitrobenzene-1-carbothioamide

HRID 987049
ノート
印刷プレビュー

反応式

HRID 987049 の反応式
COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:10])=CC=1.[N+:23]([C:26]1[CH:34]=[CH:33][C:29]([C:30]([NH2:32])=O)=[CH:28][CH:27]=1)([O-:25])=[O:24].O>O1CCOCC1>[N+:23]([C:26]1[CH:34]=[CH:33][C:29]([C:30](=[S:10])[NH2:32])=[CH:28][CH:27]=1)([O-:25])=[O:24]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 120914-NitrobenzamideHCID 87949Lawesson's reagent

生成物 1

HCID 30005644-Nitrobenzene-1-carbothioamide収率 119.3%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

6.06 g (15 mmol) of Lawesson reagent is added to a solution of 4.15 g (25 mmol) of 4-nitrobenzamide in 100 ml of 1,4-dioxan. The reaction mixture is heated under reflux for two hours. After the solution has returned to ambient temperature, it is poured into 150 ml of water and extracted with 5 times 100 ml of ethyl acetate. The organic solution is dried over magnesium sulphate, filtered and concentrated under vacuum in order to produce a yellow oil which is purified on a silica gel column (eluant: heptane/ethyl acetate 1/1). The pure fractions are collected and concentrated under vacuum. 3.26 g of a yellow powder is obtained with a yield of 72%. Melting point: 165-167° C.

後処理

  1. temperatureThe reaction mixture is heated
  2. temperatureunder reflux for two hours
  3. customhas returned to ambient temperature
  4. extractionextracted with 5 times 100 ml of ethyl acetate
  5. dry with materialThe organic solution is dried over magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated under vacuum in order
  8. customto produce a yellow oil which
  9. customis purified on a silica gel column (eluant: heptane/ethyl acetate 1/1)
  10. customThe pure fractions are collected
  11. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-2c4a48306fe446aebbb9f9c5ecc8818a
出典データセット
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06630461B2

反応ノート

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