Formic Acid → 1-Methylcyclopentane-1-carboxylic acid
Reaction equation
[CH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]=1.[CH:7]([OH:9])=[O:8]>S(=O)(=O)(O)O>[CH3:1][C:6]1([C:7]([OH:9])=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Cyclohexene (25 ml, 0.246 mol) was treated with conc. sulphuric acid (100 ml) and formic acid (18.9 ml, 0.5 mol) at 5° C. for two hours. The mixture was poured onto ice and extracted twice with EtOAc. The organic extracts were washed with brine, then extracted with 2M KOH. The basic extract was acidified with 2M HCl and extracted with CHCl3, filtered (Whatman® 1 PS phase separator) and evaporated. The resultant brown oil was purified by bulb-to-bulb distillation (125° C./oil pump) to give the title compound as a colourless oil (860 mg, 2%).
Workup
- additionThe mixture was poured onto ice
- extractionextracted twice with EtOAc
- washThe organic extracts were washed with brine
- extractionextracted with 2M KOH
- extractionThe basic extract
- extractionextracted with CHCl3
- filtrationfiltered (Whatman® 1 PS phase separator)
- customevaporated
- distillationThe resultant brown oil was purified by bulb-to-bulb distillation (125° C./oil pump)
Sources & evidence
- ORD record
- ord-d008b4dab0434bd3884a69b4f0652467
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688943
Reaction notes
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