Sulfuric Acid → HCID 22606873, compound
Reaction equation
[CH2:1]([C:3]1([C:8]2[CH:13]=[CH:12][C:11]([C:14]3[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][O:21][C:22]4[CH:23]=[C:24]([C:32]([O:34][CH3:35])=[O:33])[C:25](=[CH:30][CH:31]=4)[C:26]([O:28][CH3:29])=[O:27])[CH:15]=3)=[C:10]([CH3:36])[CH:9]=2)OCC[O:4]1)[CH3:2].S(=O)(=O)(O)O>CO.O>[CH3:36][C:10]1[CH:9]=[C:8]([C:3](=[O:4])[CH2:1][CH3:2])[CH:13]=[CH:12][C:11]=1[C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][O:21][C:22]2[CH:23]=[C:24]([C:32]([O:34][CH3:35])=[O:33])[C:25](=[CH:30][CH:31]=2)[C:26]([O:28][CH3:29])=[O:27])[CH:15]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
6.8 g (14 mmol) of dimethyl 4-[4′-(2-ethyl-[1,3]dioxolan-2-yl)-2′-methylbiphenyl-3-ylmethoxy]-phthalate are dissolved in 200 mL of methanol and 50 mL of water. 0.5 mL of sulphuric acid is added and the reaction medium is stirred at room temperature for 10 hours. After the usual treatment, the desired product is obtained, without purification, in the form of a colourless oil (m=6.05 g; Y=97%).
Sources & evidence
- ORD record
- ord-9703d7dda7e749b6840aacc9bdbbb4ee
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06831106B1
Reaction notes
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