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Phosphorus oxychloride → Methyl 4-(3-chloro-1,2,4-triazin-6-yl)benzoate

HRID 500217
ノート
印刷プレビュー

反応式

HRID 500217 の反応式
O=[C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)=[N:4][NH:3]1.P(Cl)(Cl)([Cl:20])=O>C(Cl)(Cl)Cl>[Cl:20][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)=[CH:6][N:7]=1
参加物反応条件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 24813Phosphorus oxychlorideHCID 59216301Methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate

生成物 1

HCID 59216349Methyl 4-(3-chloro-1,2,4-triazin-6-yl)benzoate収率 17.3%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

反応条件

温度
100 °C

実験手順

A mixture of methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate (13.4 g, 0.0580 mol), phosphoryl chloride (30 mL, 0.3 mol) in chloroform (50 mL) was refluxed (oil-bath temperature about 100° C.) for 2 h. After cooling to RT, the mixture was concentrated to remove excess phosphoryl chloride. The residue was dissolved in methylene chloride and poured into ice-water, and carefully neutralized with K2CO3. The organic layer was separated and the aqueous solution was extracted with methylene chloride. The combined organic phases were dried over Na2SO4, concentrated, and further purified by chromatography to afford the desired product (2.5 g, 17%). LCMS: (M+H)=249.9. 1H NMR (300 MHz, CDCl3): in ppm, 3.98 (s, 3H), 8.18 (d, 2H), 8.24 (d, 2H), 8.96 (s, 1H).

後処理

  1. temperatureAfter cooling to RT
  2. concentrationthe mixture was concentrated
  3. customto remove excess phosphoryl chloride
  4. dissolutionThe residue was dissolved in methylene chloride
  5. additionpoured into ice-water
  6. customThe organic layer was separated
  7. extractionthe aqueous solution was extracted with methylene chloride
  8. dry with materialThe combined organic phases were dried over Na2SO4
  9. concentrationconcentrated
  10. customfurther purified by chromatography

出典と根拠

ORDレコード
ord-1f813a8653c54376ae6f11b4566f88e3
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07767675B2

反応ノート

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