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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53422Generated: October 25, 2026

4-Bromotoluene → 4,4-Dimethyl-2-(4'-methyl-2-biphenylyl)-2-oxazoline

https://huagongshe.com/reaction/53422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromotolueneHCID 7805—
Reactant1,1-DibromoethaneHCID 11201—
ReactantAmmonium ChlorideHCID 25517—
Reactant4,4-Dimethyl-2-(2-methoxyphenyl)oxazolineHCID 333189—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product4,4-Dimethyl-2-(4'-methyl-2-biphenylyl)-2-oxazolineHCID 68830185.1%

Reaction Steps

Tetrahydrofuran (200 ml) was added to 2.5 g (103 mmol) of flaky magnesium, followed by the addition of a small amount of dibromoethane under stirring. After the confirmation of bubbling, 13 ml (106 mmol) of 4-bromotoluene was dropwise added thereto. After the confirmation of the dissolution of the magnesium, the mixture was further stirred at room temperature for one hour. This reaction liquid was dropwise added to a solution of 10.0 g (48.7 mmol) of 4,4-dimethyl-2-(2'-methoxyphenyl)oxazoline in tetrahydrofuran (100 ml), followed by stirring for 12 hours. The reaction liquid was poured into a saturated aqueous solution of ammonium chloride, followed by the extraction with chloroform. After washing with water and drying, vacuum concentration was conducted. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 11.0 g of the title compound as a crystal (yield 85%). m.p.; 56°-59° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618969
Source datasetuspto-grants-1997_04
ORD IDord-c2dbefa41b844817bc4dce80250238a3
Source noteuspto-grants-1997_04