反応 #42840

ord-cf9f3e4130dd49c5864e4fef290d66b4

反応方程式

[Cl-].[NH4+]
ammonium chloride
Clc1cc(Cl)ncn1
4,6-dichloropyrimidine
[H-].[Na+]
sodium hydride
CC#CCO
2-butyn-1-ol
CC#CCOc1cc(Cl)ncn1
4-chloro-6-(2-butynyloxy) pyrimidine
収率 85.9%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGstirred for 4 hours
  2. 2
    抽出the mixture was extracted with chloroform three times
  3. 3
    洗浄The organic layers were washed with water
  4. 4
    乾燥dried over anhydrous magnesium sulfate
  5. 5
    濃縮concentrated

実験手順

1.05 g of sodium hydride (60% oil suspension) was suspended in 24 ml of tetrahydrofuran. 8 ml of tetrahydrofuran solution of 1.42 g of 2-butyn-1-ol was added dropwise at room temperature therein slowly, and the mixture was stirred for 20 minutes. Into the mixture was added dropwise 8 ml of tetrahydrofuran solution of 3 g of 4,6-dichloropyrimidine at 0° C. slowly, and stirred for 4 hours. The reaction mixture was poured into a saturated ammonium chloride aqueous solution, and the mixture was extracted with chloroform three times. The organic layers were washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 3.16 g of 4-chloro-6-(2-butynyloxy) pyrimidine.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07732448B2uspto-grants-2010_06