Ethanol → HCID 57890274, compound
Reaction equation
[Si]([O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([C:34]3[CH:39]=[CH:38][C:37]([O:40][CH3:41])=[CH:36][CH:35]=3)(O)[CH:14]([C:19]3[CH:24]=[CH:23][C:22]([O:25][Si](C(C)(C)C)(C)C)=[CH:21][CH:20]=3)[CH2:15][O:16]2)=[CH:11][CH:10]=1)(C(C)(C)C)(C)C.CC1C=CC(S(O)(=O)=O)=CC=1.C(O)C>CO>[OH:25][C:22]1[CH:21]=[CH:20][C:19]([C:14]2[CH2:15][O:16][C:17]3[C:12]([C:13]=2[C:34]2[CH:39]=[CH:38][C:37]([O:40][CH3:41])=[CH:36][CH:35]=2)=[CH:11][CH:10]=[C:9]([OH:8])[CH:18]=3)=[CH:24][CH:23]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
7(tert-Butyldimethylsilyloxy)-3-(4-(tert-butyldimethylsilyloxy)phenyl)-4-(4-methoxyphenyl)chroman-4-ol (42 g), pTsOH (435 g), boiling chips and 2.5 L of ethanol were combined in a 2-neck 5 L round bottom flask with condenser attached. The reaction was heated at reflux for 3 hours. The solvent was concentrated in vacuo to ˜100 ml before being poured into chilled, stirred water (700 ml). The mixture was then extracted with ethyl acetate, the combined organic layers washed with water (3×2 L), brine (1×500 ml), dried over anhydrous magnesium sulphate and filtered and solvent removed in vacuo to give red/brown oil. The oil was dissolved in methanol (˜100 ml) and put in freezer overnight.
Workup
- customwere combined in a 2-neck 5 L round bottom flask with condenser
- temperatureThe reaction was heated
- temperatureat reflux for 3 hours
- concentrationThe solvent was concentrated in vacuo to ˜100 ml
- additionbefore being poured
- temperatureinto chilled
- extractionThe mixture was then extracted with ethyl acetate
- washthe combined organic layers washed with water (3×2 L), brine (1×500 ml)
- dry with materialdried over anhydrous magnesium sulphate
- filtrationfiltered
- customsolvent removed in vacuo
- customto give red/brown oil
Sources & evidence
- ORD record
- ord-e15cb73a2088445ebca2e01886f1d1bb
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08080675B2
Reaction notes
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