1-Propanol → Propyl 2-hydroxy-3-naphthoate

HRID 228733Notes

Reaction equation

HRID 228733 reaction equation
[OH:1][C:2]1[C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1.S(Cl)(Cl)=O.[CH2:19](O)[CH2:20][CH3:21]>>[OH:1][C:2]1[C:11]([C:12]([O:14][CH2:19][CH2:20][CH3:21])=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1

Participants

4

Conditions

Temperature
120 °C

Procedure

2-Hydroxy-naphthalene-3-carboxylic acid (2 g) was dissolved in 1-propanol (10 ml) to prepare a solution. The solution was brought to 0° C., and thionyl chloride (1.16 ml) was gradually added dropwise. The mixture was stirred at 120° C. for 2 hr. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform to give propyl 2-hydroxy-3-naphthoate (2.15 g, yield 88%).

Workup

  1. customto prepare a solution
  2. customwas brought to 0° C.
  3. temperatureThe reaction solution was cooled to room temperature
  4. customthe solvent was removed by distillation under the reduced pressure
  5. additionWater was then added to the residue
  6. extractionthe mixture was extracted with chloroform
  7. washThe chloroform layer was washed with saturated brine
  8. dry with materialwas dried over anhydrous sodium sulfate
  9. customThe solvent was removed by distillation under the reduced pressure
  10. customthe residue was purified by column chromatography

Sources & evidence

ORD record
ord-cc80bb020c394834988726fd71a6f24a
Source dataset
uspto-grants-2009_07
Patent number
US07560558B2

Reaction notes

Loading…