Hydrochloric Acid → HCID 86707566, compound
Reaction equation
COCCOC[O:7][C:8]1[CH:9]=[C:10]([C:31]2[CH:36]=[CH:35][C:34]([O:37][CH2:38][CH2:39][CH2:40][O:41]C3CCCCO3)=[CH:33][CH:32]=2)[CH:11]=[C:12]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH2:21][CH2:22][CH2:23][O:24]C3CCCCO3)=[CH:16][CH:15]=2)[CH:13]=1.Cl>CO.O>[OH:41][CH2:40][CH2:39][CH2:38][O:37][C:34]1[CH:33]=[CH:32][C:31]([C:10]2[CH:9]=[C:8]([OH:7])[CH:13]=[C:12]([C:14]3[CH:19]=[CH:18][C:17]([O:20][CH2:21][CH2:22][CH2:23][OH:24])=[CH:16][CH:15]=3)[CH:11]=2)=[CH:36][CH:35]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
7.90 g (12.1 mmol) 3′-[5′-(2-methoxy-ethoxymethoxy)-[1,1′:3′,1″-terphenyl]-4,4″-diylbis(oxy-3,1-propanediyloxy)]bis(tetrahydro-2H-pyrane) are dissolved in 60 ml methanol, and, after addition of 9 ml conc. hydrochloric acid, stirred overnight at RT. The mixture is diluted with water and extracted three times with MTB ether. The combined organic layers are washed with sat. aq. sodium chloride solution and dried over sodium sulfate. 4,4″-Bis-(3-hydroxy-propoxy)-[1,1′;3′,1″]terphenyl-5′-ol is obtained as a yellow oil.
Workup
- extractionextracted three times with MTB ether
- washThe combined organic layers are washed with sat. aq. sodium chloride solution
- dry with materialdried over sodium sulfate
Sources & evidence
- ORD record
- ord-c9bdc42494754f3caf93bbb7fcb2adb0
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133395B2
Reaction notes
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