4-Isopropylphenol → HCID 54011065, compound

HRID 1704145Notes

Reaction equation

HRID 1704145 reaction equation
Br[CH:2]([C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH:15]([O:17][C:18]2[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=2)[CH3:16])=[CH:9][CH:8]=1)[C:3]([O:5][CH3:6])=[O:4].[CH:25]([C:28]1[CH:33]=[CH:32][C:31]([OH:34])=[CH:30][CH:29]=1)([CH3:27])[CH3:26]>O1CCCC1>[CH:25]([C:28]1[CH:33]=[CH:32][C:31]([O:34][CH:2]([C:7]2[CH:12]=[CH:11][C:10]([O:13][CH2:14][CH:15]([O:17][C:18]3[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=3)[CH3:16])=[CH:9][CH:8]=2)[C:3]([O:5][CH3:6])=[O:4])=[CH:30][CH:29]=1)([CH3:27])[CH3:26]

Participants

4

Reactant 2

HCID 74654-IsopropylphenolHCID 54386710HCID 54386710, compound

Product 1

HCID 54011065HCID 54011065, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

As described in Example 71, methyl bromo{p-[2-(p-fluorophenoxy)propoxy]phenyl}acetate (0.017 mole) is reacted with p-isopropylphenol (0.017 mole) in 75 ml of tetrahydrofuran at 80° C. for 18 hrs to give the product as a viscous oil.

Sources & evidence

ORD record
ord-c1807261dbb141aeb077e8d76e09a297
Source dataset
uspto-grants-1978_11
Patent number
US04125732

Reaction notes

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