4-Methoxybenzophenone → 1,2-bis(p-methoxyphenyl)-1,2-diphenyl-1,2-ethanediol

HRID 962369Notes

Reaction equation

HRID 962369 reaction equation
[CH3:1][O:2][C:3]1[CH:16]=[CH:15][C:6]([C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:8])=[CH:5][CH:4]=1>C(O)(=O)C.C(O)(C)C>[CH3:1][O:2][C:3]1[CH:16]=[CH:15][C:6]([C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)([OH:8])[C:7]([C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:16][CH:15]=2)([C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[OH:8])=[CH:5][CH:4]=1

Participants

4

Procedure

0.04 g of acetic acid was added to 35.98 g of isopropyl alcohol, and 4.02 g of 4-methoxybenzophenone was dissolved therein. To this solution, ultraviolet rays were irradiated by a high pressure mercury lamp (UVL-100HA, manufactured by Riko Kagaku Sangyo K.K.) to carry out the reaction for 4 hours. After the reaction, the solvent was distilled off to obtain 4.01 g of 1,2-bis(p-methoxyphenyl)-1,2-diphenyl-1,2-ethanediol (compound (C2)).

Workup

  1. dissolutionwas dissolved
  2. customTo this solution, ultraviolet rays were irradiated by a high pressure mercury lamp (UVL-100HA, manufactured by Riko Kagaku Sangyo K.K.)
  3. customthe reaction for 4 hours
  4. customAfter the reaction
  5. distillationthe solvent was distilled off

Sources & evidence

ORD record
ord-0a3fe8f6e7264367ae66ccded5852d24
Source dataset
uspto-grants-1998_06
Patent number
US05759736

Reaction notes

Loading…