Pyrogallol → HCID 20092283, compound
Reaction equation
[C:1]1([CH:9]=[CH:8][CH:7]=[C:5]([OH:6])[C:3]=1[OH:4])[OH:2].[CH:10]([O:13][CH2:14]Cl)([CH3:12])[CH3:11]>>[CH:10]([O:13][CH2:14][O:2][C:1]1[CH:9]=[CH:8][CH:7]=[C:5]([O:6][CH2:14][O:13][CH:10]([CH3:12])[CH3:11])[C:3]=1[O:4][CH2:14][O:13][CH:10]([CH3:12])[CH3:11])([CH3:12])[CH3:11]Participants
3
Procedure
Using pyrogallol in place of phloroglucinol used in Synthesis Example 13 and isopropoxymethylchloride obtained in Synthesis Example 2, the reaction and treatment were carried out in the same manner as described in Synthesis Example 13 to give the corresponding 1,2,3-tris(isopropoxymethoxy)benzene as a yellow oil.
Workup
- customobtained in Synthesis Example 2
- customthe reaction and treatment
- customas described in Synthesis Example 13
Sources & evidence
- ORD record
- ord-44542bb48004437da041e3641dfd9e29
- Source dataset
- uspto-grants-1995_02
- Patent number
- US05389491
Reaction notes
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