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

HRID 916656
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HRID 916656 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178433211HCID 178433211, 화합물

생성물 1

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

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온도
100 °C

실험 절차

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.

후처리

  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)
  • 출처 및 근거

    ORD 기록
    ord-75b33cc552fe4de9a9172e78d7782f42
    출처 데이터셋
    uspto-grants-2007_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07271170B2

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