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

HRID 2071970Notes

Reaction equation

HRID 2071970 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 1/2 hour). 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-c493a3e66b5c475eb6d717cc24d3645c
Source dataset
uspto-grants-1977_09
Patent number
US04049653

Reaction notes

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