Thionyl Chloride → 3-Methylfuran-2-carbonyl chloride
Reaction equation
[CH3:1][C:2]1[CH:6]=[CH:5][O:4][C:3]=1[C:7]([OH:9])=O.S(Cl)([Cl:12])=O>C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH:6]=[CH:5][O:4][C:3]=1[C:7]([Cl:12])=[O:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Methyl-2-furancarbonyl chloride was prepared by refluxing 3-methyl-2-furancarboxylic acid (20.0 g) with thionyl chloride (25 ml) in toluene (75 ml) for 3 hours. After removal of the solvent, the acid chloride was distilled (b.p. 74°-76° C. at ca. 12 mm).
Workup
- customAfter removal of the solvent
- distillationthe acid chloride was distilled (b.p. 74°-76° C. at ca. 12 mm)
Sources & evidence
- ORD record
- ord-f64822d702a043b690ce1a55d07162f8
- Source dataset
- uspto-grants-1997_12
- Patent number
- US05693827
Reaction notes
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