Water → 1-(4-Methoxyphenyl)-3-phenylindane-2-carboxylic acid

HRID 862913Notes

Reaction equation

HRID 862913 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:10]2[C:24]([O:26]CC)=[O:25])=[CH:5][CH:4]=1.[OH-].[Na+].O>CCO>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH:10]2[C:24]([OH:26])=[O:25])=[CH:5][CH:4]=1

Participants

5

Procedure

To a solution of ethyl(1RS,2S R,3SR)-1-(4-methoxyphenyl)-3-phenylindane-2-carboxylate, (5.5 g, 14.8 mmol) in EtOH (70 ml) was added 5M NaOH (9 ml, 45 mmol). The resulting mixture was stirred under an argon atmosphere for 1 d, at which time H2O (70 ml) was added. The mixture was concentrated under reduced pressure. The aqueous residue was extracted with Et2O, and the Et2O extracts were discarded. The aqueous phase was acidified with 6M HCl and extracted several times with EtOAc. The combined EtOAc extracts were washed successively with H2O and saturated aqueous NaCl and dried. The solvent was removed in vacuo to provide an oily residue which crystallized upon standing. The solid material was recrystallized from EtOAc/hexanes to afford the title compound (4.25 g, 83%); m.p. 164°-166° C.

Workup

  1. additionwas added
  2. concentrationThe mixture was concentrated under reduced pressure
  3. extractionThe aqueous residue was extracted with Et2O
  4. extractionextracted several times with EtOAc
  5. washThe combined EtOAc extracts were washed successively with H2O and saturated aqueous NaCl
  6. customdried
  7. customThe solvent was removed in vacuo
  8. customto provide an oily residue which
  9. customcrystallized
  10. customThe solid material was recrystallized from EtOAc/hexanes

Sources & evidence

ORD record
ord-718062c9ae69492aa645f822f59d3be9
Source dataset
uspto-grants-1998_02
Patent number
US05719182

Reaction notes

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