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

HRID 1099075
ノート
印刷プレビュー

反応式

HRID 1099075 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 heated at reflux (oil-bath temperature about 100° C.) for 2 h. After cooling, the mixture was concentrated to remove excess phosphoryl chloride. The residue was dissolved in DCM. The solution was poured into ice-water, and carefully neutralized with K2CO3. The organic layer was separated. The aqueous solution was extracted with methylene chloride. The combined extracts were dried over Na2SO3. After filtration the filtrate was concentrated and further purified by flash column to afford the desired product (2.5 g, 17%). Analytical LCMS: (M+H)+=249.9. 1H NMR (300 MHz, CDCl3): 6 (ppm) 3.98 (s, 3H), 8.18 (d, 2H), 8.24 (d, 2H), 8.96 (s, 1H).

後処理

  1. temperaturewas heated
  2. temperatureAfter cooling
  3. concentrationthe mixture was concentrated
  4. customto remove excess phosphoryl chloride
  5. dissolutionThe residue was dissolved in DCM
  6. additionThe solution was poured into ice-water
  7. customThe organic layer was separated
  8. extractionThe aqueous solution was extracted with methylene chloride
  9. dry with materialThe combined extracts were dried over Na2SO3
  10. filtrationAfter filtration the filtrate
  11. concentrationwas concentrated
  12. customfurther purified by flash column

出典と根拠

ORDレコード
ord-324cc727c17f49048b7cfe56a93def64
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08143251B2

反応ノート

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