반응 #83011

ord-760aa76627d84edfb1a7dfe8d27792cc

반응 방정식

Cl
HCl
O=[N+]([O-])c1ccc(O)cc1
4-nitrophenol
O=C(Cl)CC(F)=C(F)F
3,4,4-trifluoro-3-butenoyl chloride
CCN(CC)CC
triethylamine
O=C(CC(F)=C(F)F)Oc1ccc([N+](=O)[O-])cc1
product
수율 92.1%
O=C(CC(F)=C(F)F)Oc1ccc([N+](=O)[O-])cc1
3,4,4-trifluoro-3-butenoic acid, 4-nitrophenyl ester
수율 92.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe mixture is stirred at -78° C. for 10 min
  2. 2
    기타to reach room temperature
  3. 3
    세척The organic layer is successively washed with water, 5% sodium bicarbonate, brine
  4. 4
    기타dried
  5. 5
    기타The dark brown residue obtained
  6. 6
    기타after evaporation of the solvent
  7. 7
    기타was purified

실험 절차

A solution of 4-nitrophenol (1.10 g, 0.0079 mole) and 3,4,4-trifluoro-3-butenoyl chloride (1.85 g, 0.0116 mole) in dry ether (15 mL) is treated dropwise with triethylamine (1.01 g, 0.01 mole) at -78° C. with stirring. The mixture is stirred at -78° C. for 10 min and allowed to reach room temperature. The reaction mixture is diluted with ether (20 mL), stirred with 15 mL of 2 N HCl. The organic layer is successively washed with water, 5% sodium bicarbonate, brine, and dried. The dark brown residue obtained after evaporation of the solvent was purified by passing through a short column of silica gel to give 1.9 g of the product as a brown solid, a 91% yield. m.p. 58°-62° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05623084uspto-grants-1997_04