4-tert-Butylphenol → HCID 53839438, compound

HRID 1704142Notes

Reaction equation

HRID 1704142 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].[C:25]([C:29]1[CH:34]=[CH:33][C:32]([OH:35])=[CH:31][CH:30]=1)([CH3:28])([CH3:27])[CH3:26]>O1CCCC1>[C:25]([C:29]1[CH:30]=[CH:31][C:32]([O:35][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:33][CH:34]=1)([CH3:28])([CH3:26])[CH3:27]

Participants

4

Reactant 2

HCID 73934-tert-ButylphenolHCID 54386710HCID 54386710, compound

Product 1

HCID 53839438HCID 53839438, 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 2.55 g of p-tert-butylphenol in 75 ml of tetrahydrofuran at 80° C. for 18 hrs to give the product as a gum.

Sources & evidence

ORD record
ord-b2d91bb5beb148ec986b51d4d432085a
Source dataset
uspto-grants-1978_11
Patent number
US04125732

Reaction notes

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