반응 #4882

ord-bbe4662ee3c84951be6a4e98c39cf4dd

반응 방정식

O=C=O
dry ice
CC(C)NC(C)C
diisopropylamine
[Li][CH2]CCC
n-butyllithium
Clc1cncc(Cl)c1
3,5-dichloropyridine
O=C(O)c1c(Cl)cncc1Cl
3,5-Dichloro-4-pyridinecarboxylic acid

반응 조건

온도
-70°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도while maintaining the above temperature
  2. 2
    workup.ADDITIONTwenty minutes subsequent to that addition
  3. 3
    기타to evaporate overnight at room temperature
  4. 4
    세척washed with 3×30 ml of methylenechloride
  5. 5
    여과filtered
  6. 6
    기타to precipitate out the product
  7. 7
    온도After cooling
  8. 8
    기타the precipitate was collected
  9. 9
    기타recrystallized from ethyl acetate/hexane giving 1.9 g (29%) of white analytically pure crystals, m.p. 231°-35° C. (decomp.)

실험 절차

To a solution of 4.96 ml (0.036 mole) of diisopropylamine in 200 ml of tetrahydrofuran at -65° C. under a nitrogen blanket was added dropwise 14.9 ml of 2.5M n-butyllithium in hexane while maintaining the above temperature. Twenty minutes subsequent to that addition, a solution 5.0 g (0.034 mole) of 3,5-dichloropyridine in 30 ml tetrahydrofuran at -60° to -70° C. was added. The reaction mixture was stirred at -70° C. for 1/2 hr, poured onto a large excess of dry ice and allowed to evaporate overnight at room temperature. The residue was taken up in 100 ml of dilute aqueous sodium hydroxide, washed with 3×30 ml of methylenechloride and filtered. The filtrate was acidified to ~pH 2 with dilute hydrochloric acid to precipitate out the product. After cooling, the precipitate was collected and recrystallized from ethyl acetate/hexane giving 1.9 g (29%) of white analytically pure crystals, m.p. 231°-35° C. (decomp.).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04727152uspto-grants-1988_02