Sulfuric Acid → HCID 57229312, compound
Reaction equation
S(=O)(=O)(O)O.O1CCCCC1[O:12][C:13]1[CH:14]=[C:15]([CH:26]=[CH:27][C:28]2[CH:29]=[C:30]([CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][C:40]([CH3:43])([OH:42])[CH3:41])[CH:31]=[CH:32][CH:33]=2)[CH:16]=[C:17]([O:19]C2CCCCO2)[CH:18]=1>C1COCC1.O>[OH:42][C:40]([CH3:43])([CH3:41])[CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][C:30]1[CH:29]=[C:28]([CH:27]=[CH:26][C:15]2[CH:14]=[C:13]([OH:12])[CH:18]=[C:17]([OH:19])[CH:16]=2)[CH:33]=[CH:32][CH:31]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
In a manner similar to Example 25(d), by reacting 0.06 ml of concentrated sulphuric acid with 1.15 g (2.21 mmol) of 8-(3-{2-[3,5-bis(tetrahydropyran-2-yloxy)phenyl]vinyl}phenyl)-2-methyloctan-2-ol in 20 ml of THF and 10 ml of water, after purification on a silica column (ethyl acetate 40-heptane 60), pinkish crystals (m=331 mg; Y=42%) are obtained.
Workup
- customafter purification on a silica column (ethyl acetate 40-heptane 60), pinkish crystals (m=331 mg; Y=42%)
- customare obtained
Sources & evidence
- ORD record
- ord-d5ae854f3a7949d197f54869996d5960
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06689922B1
Reaction notes
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