1-Octanol → Octanal
Reaction equation
ClN1C(=O)CCC1=O.[CH2:9]([OH:17])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].CCN(CC)CC>C1(C)C=CC=CC=1>[CH:9](=[O:17])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -25 °C
Procedure
To a solution of N-chlorosuccinimide (0.1 g, 0.8 mmol) in toluene (2 mL) was added flurous sulfide 1 (0.4 g, 1 mmol) at 0° C. resulting in the immediate formation of a white cloudy precipitate. The reaction mixture was cooled to −25° C., and a solution of octanol (0.07 g, 0.5 mmol) in toluene (2 mL) was added. After stirring at −25° C. for 2 hours, a solution of Et3N (0.08 g, 0.8 mmol) was added. The cold bath was removed after 5 minutes, and the reaction mixture washed with saturated aqueous NH4Cl, then water. The organic layer was extracted continuously with FC72 solvent (15 mL) in a cooled continuous extractor for a period of 4 hours. Concentration of the toluene layer and chromatography on silica gel (eluent: EtOAc/hexanes 3:1) yielded octanal (0.06 g, 88%). The FC72 layer was carefully concentrated under aspirator vacuum to give recovered fluorous sulfide 1 (0.3 g, 75%).
Workup
- customresulting in the immediate formation of a white cloudy precipitate
- customThe cold bath was removed after 5 minutes
- washthe reaction mixture washed with saturated aqueous NH4Cl
- extractionThe organic layer was extracted continuously with FC72 solvent (15 mL) in a cooled continuous extractor for a period of 4 hours
Sources & evidence
- ORD record
- ord-abfc348e20b64945a388a036161aca92
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06620972B2
Reaction notes
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