Acetic Acid → 5-[5-(4-Fluorophenyl)pentan-2-yl]benzene-1,3-diol

HRID 2398860Notes

Reaction equation

HRID 2398860 reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([CH:11]([CH2:13][CH2:14][CH2:15][C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)[CH3:12])[CH:6]=[C:7]([O:9]C)[CH:8]=1.C(O)(=O)C.Br>O>[OH:2][C:3]1[CH:4]=[C:5]([CH:11]([CH2:13][CH2:14][CH2:15][C:16]2[CH:17]=[CH:18][C:19]([F:22])=[CH:20][CH:21]=2)[CH3:12])[CH:6]=[C:7]([OH:9])[CH:8]=1

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 260Hydrogen Bromide2×HCID 202878722-(3,5-Dimethoxyphenyl)-5-(p-fluorophenyl)pentane

Product 1

HCID 202879045-[5-(4-Fluorophenyl)pentan-2-yl]benzene-1,3-diol

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Fifty grams of the above prepared 2-(3,5-dimethoxyphenyl)-5-(4-fluorophenyl)pentane, 450 ml. of acetic acid and 180 ml. of 48% HBr in water were mixed. While cooling, the mixture was saturated with hydrogen bromide gas (approximately 1/2hour). The reaction was placed in an 87° bath and stirred for 17 hours. The reaction was then concentrated in vacuo and the residue neutralized with K2CO3 and NaHCO3, extracted with ether, treated with charcoal and MgSO4 and filtered to yield 45 g. of 2-(3,5-dihydroxyphenyl)-5-(4-fluorophenyl)pentane as a brown oil which distills at 180° /0.01 mmHg.

Workup

  1. temperatureWhile cooling
  2. customwas placed in an 87°
  3. concentrationThe reaction was then concentrated in vacuo
  4. extractionextracted with ether
  5. additiontreated with charcoal and MgSO4
  6. filtrationfiltered
  7. customto yield 45 g
  8. distillationof 2-(3,5-dihydroxyphenyl)-5-(4-fluorophenyl)pentane as a brown oil which distills at 180° /0.01 mmHg

Sources & evidence

ORD record
ord-df23324609bb43e48be36567c9600f3e
Source dataset
uspto-grants-1977_05
Patent number
US04025630

Reaction notes

Loading…