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Thionyl Chloride → O-methyl (4'-methylbiphenyl-2-yl)carbonylthiocarbamate

HRID 5227
ノート
印刷プレビュー

反応式

HRID 5227 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]([OH:16])=O)=[CH:4][CH:3]=1.S(Cl)(Cl)=O.[S-:21][C:22]#[N:23].[K+].[O:25]1CCOC[CH2:26]1>C(Cl)(Cl)Cl>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]([NH:23][C:22](=[S:21])[O:25][CH3:26])=[O:16])=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 24386Thionyl ChlorideHCID 312751,4-DioxaneHCID 815682-(4-Methylphenyl)benzoic acidHCID 516872Potassium thiocyanate

生成物 1

HCID 54295303O-methyl (4'-methylbiphenyl-2-yl)carbonylthiocarbamate

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

In chloroform (40 ml) was dissolved (4'-methylbiphenyl-2-yl)carboxylic acid (10 g). To the solution was added thionyl chloride (7 ml), and the mixture was heated for 3 hours under reflux. The reaction mixture was poured into ice-water, then the organic layer was separated, washed with water and concentrated to dryness to give a syrup, which was dissolved in dioxane (80 ml). To the solution was added powdered potassium thiocyanate (9.16 g), and the mixture was heated for one hour under reflux. The reaction mixture was allowed to cool, and then insolubles were filtered off. After addition of methanol (15 ml) to the filtrate, the solution was heated for 15 minutes under reflux. The reaction solution was concentrated to dryness, and the resulting crystals were crystallized from isopropyl ether to afford the title compound as white plates (7.4 g, 55%),

後処理

  1. temperaturethe mixture was heated for 3 hours
  2. temperatureunder reflux
  3. customthe organic layer was separated
  4. washwashed with water
  5. concentrationconcentrated to dryness
  6. customto give a syrup, which
  7. temperaturethe mixture was heated for one hour
  8. temperatureunder reflux
  9. temperatureto cool
  10. filtrationinsolubles were filtered off
  11. additionAfter addition of methanol (15 ml) to the filtrate
  12. temperaturethe solution was heated for 15 minutes
  13. temperatureunder reflux
  14. concentrationThe reaction solution was concentrated to dryness
  15. customthe resulting crystals were crystallized from isopropyl ether

出典と根拠

ORDレコード
ord-3530d84ddd434b9796c4ba61b9c55ed4
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05243054

反応ノート

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