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Phosphorus trichloride → HCID 501246、化合物

HRID 2300998
ノート
印刷プレビュー

反応式

HRID 2300998 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[CH:9]([S:11]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N+:15]=1[O-])(=[O:13])=[O:12])[CH3:10].P(Cl)(Cl)Cl>C(Cl)(Cl)Cl>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[CH:9]([S:11]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1)(=[O:12])=[O:13])[CH3:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24387Phosphorus trichlorideHCID 501133Dimenoxypyrin

生成物 1

HCID 501246HCID 501246、化合物

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

A mixture of 4.7 g (0.017 mole) of 2-[1-(2,5-Dimethylphenyl)-ethylsulfonyl]-pyridine-N-oxide, 60 ml of chloroform, and 7.5 g (0.055 mole) of PCl3 were placed in a 100 ml round bottom flask equipped with a magnetic stirrer and reflux condenser. The mixture was refluxed for one hour, and then the solvent was removed under reduced pressure using a rotovap. To the residue was added 25 ml of ethanol, followed by a second evaporation. The residue crystallized to give a white solid, which was recrystallized from ethanol. Obtained were 3.0 g of product having a melting point of 95-96° C. The IR, NMR and mass spectra were consistent with the proposed structure.

後処理

  1. customwere placed in a 100 ml round bottom flask
  2. customequipped with a magnetic stirrer
  3. temperaturereflux condenser
  4. temperatureThe mixture was refluxed for one hour
  5. customthe solvent was removed under reduced pressure
  6. additionTo the residue was added 25 ml of ethanol
  7. customfollowed by a second evaporation
  8. customThe residue crystallized
  9. customto give a white solid, which
  10. customwas recrystallized from ethanol
  11. customObtained

出典と根拠

ORDレコード
ord-c96ba3c5839742578ac2fde5cebb90f3
出典データセット
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06498254B1

反応ノート

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