Hydrochloric Acid → Ethyl [p-(p-nitrophenoxy)phenyl]acetate
Reaction equation
[N+:1]([C:4]1[CH:20]=[CH:19][C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][C:16]([OH:18])=[O:17])=[CH:11][CH:10]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].Cl.O.[CH2:23](O)[CH3:24]>>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][C:16]([O:18][CH2:23][CH3:24])=[O:17])=[CH:11][CH:10]=2)=[CH:19][CH:20]=1)([O-:3])=[O:2]Participants
Procedure
A solution of 27.3 g of [p-(p-nitrophenoxy)phenyl]acetic acid in 270 ml of ethanol is cooled to 0° C. and saturated with dry HCl gas over 31/2 hours. The resulting deep red solution is heated to reflux and maintained at reflux overnight. A yellow crystalline solid separates on cooling. The entire mixture is poured into 500 ml of water and extracted with three 200 ml portions of benzene. The combined extracts are washed with two 150 ml portions of water, two 150 ml portions of saturated NaHCO3, 150 ml of saturated brine, and dried over MgSO4. Evaporation of the solvent at reduced pressure affords an oil which yields yellow crystals from 50 ml of ethanol, mp 70.5°-73° C. Recrystallization from ethanol affords yellow prisms, mp 70.5°-73° C.
Workup
- temperatureThe resulting deep red solution is heated
- temperatureto reflux
- temperaturemaintained
- temperatureat reflux overnight
- temperatureA yellow crystalline solid separates on cooling
- extractionextracted with three 200 ml portions of benzene
- washThe combined extracts are washed with two 150 ml portions of water, two 150 ml portions of saturated NaHCO3, 150 ml of saturated brine
- dry with materialdried over MgSO4
- customEvaporation of the solvent at reduced pressure
- customaffords an oil which
- customRecrystallization from ethanol
- customaffords yellow prisms, mp 70.5°-73° C.
Sources & evidence
- ORD record
- ord-1fc4fca6921d4131a0e6bdb76497c61e
- Source dataset
- uspto-grants-1979_09
- Patent number
- US04168385
Reaction notes
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