4-Hydroxybenzoic Acid → Benzoic acid, 4-hydroxy-, 2-methylbutyl ester

HRID 1612581Notes

Reaction equation

HRID 1612581 reaction equation
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[CH3:11][C@@H:12]([CH2:15][CH3:16])[CH2:13]O.S(=O)(=O)(O)O.O>C1(C)C=CC=CC=1>[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH2:11][CH:12]([CH3:13])[CH2:15][CH3:16])=[O:7])=[CH:4][CH:3]=1

Participants

6

Reactant 4

HCID 1354-Hydroxybenzoic AcidHCID 962WaterHCID 1118Sulfuric AcidHCID 2723602(S)-2-methyl-1-butanol

Product 1

HCID 13530949Benzoic acid, 4-hydroxy-, 2-methylbutyl esterYield 83%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

4.0 g of p-hydroxybenzoic acid and 12.5 g of (S)-(-)-2-methylbutanol were refluxed for 6 hours in toluene in the presence of sulfuric acid, while the generated water was removed out. Subsequently, the reaction solution was washed with water to remove sulfuric acid out. After the resulting solution was dried and concentrated, the concentrate was purified by column chromatography to obtain 5.0 g of the objective ester compound (liquid state at room temperature, [α]D23 =+4.9° (CHCl3)). (Yield: 83%)

Workup

  1. customwas removed out
  2. washSubsequently, the reaction solution was washed with water
  3. customto remove sulfuric acid out
  4. customAfter the resulting solution was dried
  5. concentrationconcentrated
  6. customthe concentrate was purified by column chromatography

Sources & evidence

ORD record
ord-3026b880b4bd479eb7f10a251215cf5a
Source dataset
uspto-grants-1993_03
Patent number
US05190686

Reaction notes

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