Methanol → Penclomedine

HRID 2413468

反応式

HRID 2413468 の反応式
Cl[C:2]1[C:7]([Cl:8])=[C:6](Cl)[C:5]([Cl:10])=[C:4]([C:11]([Cl:14])([Cl:13])[Cl:12])[N:3]=1.[CH3:15][OH:16].[CH3:17][O-:18].[Na+]>CS(C)=O>[Cl:8][C:7]1[C:2]([O:18][CH3:17])=[N:3][C:4]([C:11]([Cl:14])([Cl:13])[Cl:12])=[C:5]([Cl:10])[C:6]=1[O:16][CH3:15]

参加物

5

実験手順

A 50.0 g portion (0.15 mol) of 2,3,4,5-tetrachloro-6-(trichloromethyl)pyridine was dissolved in 50 ml of warm dimethyl sulfoxide and 100 ml of methanol was added. Sodium methoxide (68.5 ml of 25 percent solution in methanol, 0.30 mol) was added, with stirring, over a 30 minute period and the resulting mixture was heated to reflux, with stirring, for two hours. After cooling, the mixture was poured into ice water and the aqueous mixture was extracted twice with methylene chloride. The extract was washed with water and evaporated to remove the methylene chloride. Traces of dimethyl sulfoxide remained. The residue was dissolved in ether and the ethereal solution was washed with water, dried over magnesium sulfate, and evaporated under reduced pressure to obtain 39.4 g of white solid product (81 percent of theory) melting at 67°-69° C. The proton nmr spectrum was consistent with the structure given.

後処理

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux
  3. stirringwith stirring, for two hours
  4. temperatureAfter cooling
  5. extractionthe aqueous mixture was extracted twice with methylene chloride
  6. washThe extract was washed with water
  7. customevaporated
  8. customto remove the methylene chloride
  9. dissolutionThe residue was dissolved in ether
  10. washthe ethereal solution was washed with water
  11. dry with materialdried over magnesium sulfate
  12. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-fd1322b11ed8470093839001a6f2fbef
出典データセット
uspto-grants-1988_01
特許番号
US04717726

関連ノート

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