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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163788Generated: October 25, 2026

1,2-Dimethoxyethane → 2-[4-(Hexadecylamino)phenyl]oxazoline

https://huagongshe.com/reaction/2163788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
Reactant2-Bromoethylamine hydrobromideHCID 2774217—
Reactant4-Hexadecylaminobenzoyl chloride hydrochlorideHCID 13255322—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTriethylamineHCID 8471—
Product2-[4-(Hexadecylamino)phenyl]oxazolineHCID 20437370—

Reaction Steps

To a slurry of 15 g. of 2-bromoethylamine hydrobromide in 150 ml. of glyme was added simultaneously solutions of 31 g. of 4-(hexadecylamino)benzoyl chloride hydrochloride in 60 ml. of glyme and 50 cc. of triethylamine (dropwise). Upon addition of 0.5 g. of 4-dimethylaminopyridine the "solution" was stirred at room temperature overnight. The solution was refluxed for one hour and filtered. The solid was oven dried and portitioned between CH2Cl and water. The layers were separated and the organic phase dried over MgSO4. The organic layer was concentrated to about 100 ml. and 4-(hexadecylamino)benzoyl chloride hydrochloride diluted with an equal volume of hexane. The combined product (4.15 g.) was preabsorbed on 40 g. of silica III and placed on a column of silica III (800 g.). Fractions were collected by U.V. (CH2Cl2 --EtOH 97-3) and samples with the same TLC combined giving 3.8 g. after recrystallization from cyclohexane. A 210 mg. sample was recrystallized from acetonitrile and CH2Cl2 /hexane giving 149 mg., m.p. 123°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04136256
Source datasetuspto-grants-1979_01
ORD IDord-8718fe05108841e99727674bbeb5add6
Source noteuspto-grants-1979_01