Hydrochloric Acid → HCID 69492514, compound
Reaction equation
[CH2:1]([O:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]=[CH:15][C:16]2[CH:38]=[CH:37][C:19]([CH2:20][O:21][CH2:22][CH:23]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)[O:24][C@@H]3CCCCO3)=[CH:18][CH:17]=2)=[CH:10][CH:9]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].Cl>C(O)C>[C:31]1([C@@H:23]([OH:24])[CH2:22][O:21][CH2:20][C:19]2[CH:37]=[CH:38][C:16](/[CH:15]=[CH:14]/[C:11]3[CH:10]=[CH:9][C:8]([O:7][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])=[CH:13][CH:12]=3)=[CH:17][CH:18]=2)[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.4 g of (R)-2-(2-{4-[2-(4-Hexyloxy-phenyl)-vinyl]-benzyloxy}-1-phenyl-ethoxy)-tetrahydro-pyran (4) were dissolved in 30 ml of ethanol. Hydrochloric acid was added dropwise to obtain an acidic medium. Then the mixture was refluxed for 30 min. Upon cooling the product crystallized. The solid was filtered, washed with ethanol, and dried in a dessicator.
Workup
- customto obtain an acidic medium
- temperatureThen the mixture was refluxed for 30 min
- temperatureUpon cooling the product
- customcrystallized
- filtrationThe solid was filtered
- washwashed with ethanol
- customdried in a dessicator
Sources & evidence
- ORD record
- ord-d8c43d69f3a24429a8b8bed72d8f637d
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07261836B2
Reaction notes
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