Sulfuric Acid → HCID 22606873, compound

HRID 2307578Notes

Reaction equation

HRID 2307578 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]=1

Participants

5

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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