反応 #63734

ord-3e8c259a6f7645cdae3e0abea5f224a9

反応方程式

CCCOc1cc[n+]([O-])c(C)c1C
2,3-dimethyl-4-propoxypyridine 1-oxide
O=C(Cl)C(Cl)(Cl)Cl
trichloroacetyl chloride
O=C(Cl)C(Cl)(Cl)Cl
trichloroacetyl chloride
O=C=O
carbon dioxide
CCOCC
ether
CCCOc1ccnc(CCl)c1C.Cl
2-chloromethyl-3-methyl-4-propoxypyridine hydrochloride

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux temperature (oil-bath 130° )
  2. 2
    温度cooled to 10° with ice
  3. 3
    workup.STIRRINGstirred for 1 hour
  4. 4
    温度while cooling with ice
  5. 5
    その他The crystalline precipitate which separates during the entire reaction
  6. 6
    ろ過is filtered off under suction
  7. 7
    洗浄washed with ice-cold isopropyl acetate and ether
  8. 8
    その他Crystalline reaction product can again be obtained from the mother liquor

実験手順

A solution of 23 ml of trichloroacetyl chloride in 50 ml of isopropyl acetate is added dropwise during 1 hour to a solution, boiling at reflux under argon, of 13 g of 2,3-dimethyl-4-propoxypyridine 1-oxide in 250 ml of isopropyl acetate. At the beginning the reaction exhibits a very exothermic character. During the addition of the first mol equivalent of trichloroacetyl chloride a vigorous evolution of carbon dioxide is observed. The solution is subsequently stirred under argon for a further 15 minutes at reflux temperature (oil-bath 130° ), cooled to 10° with ice. treated with 100 ml of ether and stirred for 1 hour while cooling with ice. The crystalline precipitate which separates during the entire reaction is filtered off under suction and washed with ice-cold isopropyl acetate and ether. Crystalline reaction product can again be obtained from the mother liquor. The 2-chloromethyl-3-methyl-4-propoxypyridine hydrochloride obtained is processed directly.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04766133uspto-grants-1988_08