تفاعل #42840

ord-cf9f3e4130dd49c5864e4fef290d66b4

معادلة التفاعل

[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
المردود 85.9%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred for 4 hours
  2. 2
    استخلاصthe mixture was extracted with chloroform three times
  3. 3
    غسيلThe organic layers were washed with water
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    تركيزconcentrated

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07732448B2uspto-grants-2010_06