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Phosphorus oxychloride → 2-Methyl-5-propyl-6-chloro-pyrimidine-4-carboxylic acid ethyl ester

HRID 965685
ノート
印刷プレビュー

反応式

HRID 965685 の反応式
[CH2:1]([O:3][C:4]([C:6]1[C:11]([CH2:12][CH2:13][CH3:14])=[C:10](O)[N:9]=[C:8]([CH3:16])[N:7]=1)=[O:5])[CH3:2].O=P(Cl)(Cl)[Cl:19]>>[CH2:1]([O:3][C:4]([C:6]1[C:11]([CH2:12][CH2:13][CH3:14])=[C:10]([Cl:19])[N:9]=[C:8]([CH3:16])[N:7]=1)=[O:5])[CH3:2]
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

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 178439777HCID 178439777、化合物

生成物 1

HCID 233941042-Methyl-5-propyl-6-chloro-pyrimidine-4-carboxylic acid ethyl ester

反応条件

温度
85 °C

実験手順

A mixture of 2-methyl-5-propyl-6-hydroxy-pyrimidine-4-carboxylic acid ethyl ester (10 mmol) and POCl3 (25 mL) is heated at 85° C. for 4 hours. The solvent is removed in vacuo and EtOAc (40 mL) and water (30 mL) are added to the residue. NaHCO3 is carefully added until the pH of aqueous layer is greater than 7. The layers are separated and the aqueous layer is extracted with EtOAc (2×30 mL). The combined extracts are washed with brine (50 mL), dried (Na2SO4), and evaporated. Flash column purification of the residue with 3:1 EtOAc, hexane provides 2-methyl-5-propyl-6-chloro-pyrimidine-4-carboxylic acid ethyl ester as a light yellow oil. Step 4. Preparation of 2-Methyl-5-propyl-4-chloromethyl-6-chloro-pyrimidine

後処理

  1. customThe solvent is removed in vacuo and EtOAc (40 mL) and water (30 mL)
  2. additionare added to the residue
  3. additionNaHCO3 is carefully added until the pH of aqueous layer
  4. customThe layers are separated
  5. extractionthe aqueous layer is extracted with EtOAc (2×30 mL)
  6. washThe combined extracts are washed with brine (50 mL)
  7. dry with materialdried (Na2SO4)
  8. customevaporated
  9. customFlash column purification of the residue with 3:1 EtOAc, hexane

出典と根拠

ORDレコード
ord-517ddb9926014f848dd7403fe75c1b53
出典データセット
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06951864B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート