Sulfuric Acid → HCID 67278647, compound
Reaction equation
S(=O)(=O)(O)O.C(OC[O:10][C:11]1[CH:12]=[C:13]([CH:22]=[CH:23][C:24]2[CH:25]=[C:26]([C:30]([OH:46])([CH2:32][CH2:33][CH2:34][CH2:35][C:36]([CH3:45])([O:38]C3CCCCO3)[CH3:37])[CH3:31])[CH:27]=[CH:28][CH:29]=2)[CH:14]=[C:15]([O:17]COCC)[CH:16]=1)C>CO.C1COCC1>[OH:46][C:30]([C:26]1[CH:25]=[C:24]([CH:23]=[CH:22][C:13]2[CH:12]=[C:11]([OH:10])[CH:16]=[C:15]([OH:17])[CH:14]=2)[CH:29]=[CH:28][CH:27]=1)([CH3:31])[CH2:32][CH2:33][CH2:34][CH2:35][C:36]([OH:38])([CH3:45])[CH3:37]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
In a manner similar to Example 1(j), by reacting 0.6 ml of concentrated sulphuric acid in 7.5 ml of methanol with 369 mg (0.65 mmol) of 2-{3-[2-(3,5-bis-ethoxymethoxyphenyl)vinyl}phenyl}-7-methyl-7-(tetrahydropyran-2-yloxy)octan-2-ol in 7.4 ml of THF, after purification on a silica column (ethyl acetate 70-heptane 30), a yellowish paste (m=220 mg; Y=92%) is obtained.
Workup
- customafter purification on a silica column (ethyl acetate 70-heptane 30)
- customa yellowish paste (m=220 mg; Y=92%) is obtained
Sources & evidence
- ORD record
- ord-18628a45159c4909ba4d0781474fb709
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06689922B1
Reaction notes
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