Benzene → HCID 14514923, compound
Reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10](O)[CH:11]([CH3:13])[CH3:12])=[CH:9][C:4]=2[O:3][CH2:2]1.[SH:15][CH2:16][C:17]([OH:19])=[O:18].C1(C)C=CC(S(O)(=O)=O)=CC=1.C1C=CC=CC=1>C(OCC)(=O)C>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH:10]([S:15][CH2:16][C:17]([OH:19])=[O:18])[CH:11]([CH3:13])[CH3:12])=[CH:9][C:4]=2[O:3][CH2:2]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture comprising 2 g of 1-(1,3-benzodioxol-5-yl)-2-methyl-1-propanol, 1.3 g of mercaptoacetic acid, a catalytic amount of p-toluenesulfonic acid and 50 ml of benzene was heated under reflux for 5.5 hours, followed by the addition of ethyl acetate. The mixture was washed with water and extracted with a 2N aqueous solution of sodium hydroxide. The aqueous layer was washed with chloroform, acidified with dilute hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, drided over anhydrous magnesium sulfate and concentrated in a vacuum to obtain a residue. This residue was purified by silica gel column chromatography (chloroform/methanol =20:1) to obtain 2.14 g of the title compound as a colorless oil.
Workup
- temperatureunder reflux for 5.5 hours
- washThe mixture was washed with water
- extractionextracted with a 2N aqueous solution of sodium hydroxide
- washThe aqueous layer was washed with chloroform
- extractionextracted with ethyl acetate
- washThe extract was washed with water
- concentrationconcentrated in a vacuum
- customto obtain a residue
- customThis residue was purified by silica gel column chromatography (chloroform/methanol =20:1)
Sources & evidence
- ORD record
- ord-2fd6bf0f49b642fe80bc337229eb3f50
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05110956
Reaction notes
Loading…