Ethanol → 4-(4-Pentenoxy)-4'-nitrobiphenyl

HRID 1607954Notes

Reaction equation

HRID 1607954 reaction equation
C(O)C.[OH:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=2)=[CH:7][CH:6]=1.[OH-].[K+].Br[CH2:23][CH2:24][CH2:25][CH:26]=[CH2:27]>O>[CH2:27]([O:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=2)=[CH:9][CH:10]=1)[CH2:26][CH2:25][CH:24]=[CH2:23]

Participants

6

Procedure

To 400 ml ethanol is added 21.5 g of 4-hydroxy-4'-nitrobiphenyl, and the mixture heated to reflux. A solution of 7.1 g KOH in 30 ml of water is added dropwise at reflux temperatures. After complete addition, 18 g of 5-bromo-1-pentene is added and the reaction medium is heated at reflux temperature for about 15 hours. Ethanol is removed under vacuum from the cooled mixture, and the solid residue is slurried with water in a blender,filtered, washed with water, and air dried. The product then is recrystallized from 90/10 hexane/toluene, mp 74°-76° C.

Workup

  1. temperaturethe mixture heated to reflux
  2. temperatureat reflux temperatures
  3. additionis added
  4. temperaturethe reaction medium is heated
  5. temperatureat reflux temperature for about 15 hours
  6. customEthanol is removed under vacuum from the cooled mixture
  7. washwashed with water, and air
  8. customdried
  9. customThe product then is recrystallized from 90/10 hexane/toluene, mp 74°-76° C.

Sources & evidence

ORD record
ord-dac2a71e6ff845dbb6eb9782dddebda5
Source dataset
uspto-grants-1989_09
Patent number
US04868250

Reaction notes

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