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Phosphorus oxychloride → 5-(2-Benzyloxy-ethyl)-4-chloro-6-methyl-pyrimidine

HRID 916656
ノート
印刷プレビュー

反応式

HRID 916656 の反応式
[CH2:1]([O:8][CH2:9][CH2:10][C:11]1[C:12](O)=[N:13][CH:14]=[N:15][C:16]=1[CH3:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O=P(Cl)(Cl)[Cl:21]>>[CH2:1]([O:8][CH2:9][CH2:10][C:11]1[C:12]([Cl:21])=[N:13][CH:14]=[N:15][C:16]=1[CH3:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=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

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 178433211HCID 178433211、化合物

生成物 1

HCID 575033065-(2-Benzyloxy-ethyl)-4-chloro-6-methyl-pyrimidine

反応条件

温度
100 °C

実験手順

A mixture of 160 (4.1 g, 17 mmol) and POCl3 (10 ml) is heated at 100° C. for 3 hours. The solvent is removed in vacuo and EtOAc (30 ml) and water (30 ml) are added to the residue. NaHCO3 (aq.) is carefully added until the pH of the 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 solvent evaporated. Flash column purification of the residue (EtOAc:hexane=1:2) provides the product (161) as a light yellow oil.

後処理

  1. customThe solvent is removed in vacuo and EtOAc (30 ml) and water (30 ml)
  • additionare added to the residue
  • additionNaHCO3 (aq.) is carefully added until the pH of the aqueous layer
  • customThe layers are separated
  • extractionthe aqueous layer is extracted with EtOAc (2×30 ml)
  • washThe combined extracts are washed with brine (50 ml)
  • dry with materialdried (Na2SO4) and solvent
  • customevaporated
  • customFlash column purification of the residue (EtOAc:hexane=1:2)
  • 出典と根拠

    ORDレコード
    ord-75b33cc552fe4de9a9172e78d7782f42
    出典データセット
    uspto-grants-2007_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07271170B2

    反応ノート

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