4-Methoxyphenol → HCID 86601934, compound
Reaction equation
[Na:1].S(CCC[CH2:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH2:19][CH2:20]CS(O)(=O)=O)=[CH:13][CH:12]=1)(O)(=O)=O.COC1C=CC(O)=CC=1.C1[S:40](=[O:42])(=[O:41])[O:39]CCC1.[Na].COC1C=CC=CC=1OCCCCS(O)(=O)=O>>[Na:1].[CH3:9][O:10][C:11]1[CH:12]=[CH:13][C:14]([O:17][CH2:18][CH2:19][CH2:20][S:40]([OH:42])(=[O:41])=[O:39])=[CH:15][CH:16]=1Participants
5
Procedure
In the same manner as in above (1), the objective compound was synthesized from 4-methoxyphenol and butanesultone. The crude product was recrystallized from water to obtain a milky white needle crystal product. The resulting product was determined for its 1H-NMR and IR spectrum to confirm that it was 1-methoxy-4-sulfobutoxybenzene sodium.
Workup
- customThe crude product was recrystallized from water
- customto obtain a milky white needle crystal product
Sources & evidence
- ORD record
- ord-673fbc8a4ee249cda099df0c235a7385
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07279244B2
Reaction notes
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