1-Propanol → Propyl 2-hydroxy-3-naphthoate
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]=1Participants
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
- customto prepare a solution
- customwas brought to 0° C.
- temperatureThe reaction solution was cooled to room temperature
- customthe solvent was removed by distillation under the reduced pressure
- additionWater was then added to the residue
- extractionthe mixture was extracted with chloroform
- washThe chloroform layer was washed with saturated brine
- dry with materialwas dried over anhydrous sodium sulfate
- customThe solvent was removed by distillation under the reduced pressure
- customthe residue was purified by column chromatography
Sources & evidence
- ORD record
- ord-cc80bb020c394834988726fd71a6f24a
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07560558B2
Reaction notes
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