Sulfuric Acid → HCID 57219182, compound
Reaction equation
S(=O)(=O)(O)O.C([Si](C)(C)[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([CH:18]=[CH:19][C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][C:31]([CH3:40])([O:33]C3CCCCO3)[CH3:32])[CH:21]=2)[CH:13]=1)(C)(C)C>C1COCC1.O>[OH:33][C:31]([CH3:40])([CH3:32])[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][C:22]1[CH:21]=[C:20]([CH:19]=[CH:18][C:14]2[CH:13]=[C:12]([OH:11])[CH:17]=[CH:16][CH:15]=2)[CH:25]=[CH:24][CH:23]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
In a manner similar to Example 25(d), by reacting 0.133 ml of concentrated sulphuric acid with 1.25 g (2.39 mmol) of tert-butyldimethyl-[3-(2-{3-[6-methyl-6-(tetrahydropyran-2-yloxy)heptyl]phenyl}-vinyl)phenoxy]silane in 20 ml of THF and 10 ml of water, after crystallization from a heptane/ethyl acetate mixture, white crystals (m=697 mg; Y=90%) are obtained. m.p.=96-7° C.
Workup
- customafter crystallization from a heptane/ethyl acetate mixture, white crystals (m=697 mg; Y=90%)
- customare obtained
Sources & evidence
- ORD record
- ord-f4304924609a4ef5a45fa2802f35bcc2
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06689922B1
Reaction notes
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