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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732846Generated: October 29, 2026

Toluene → Diethylene glycol monoglycidyl ether

https://huagongshe.com/reaction/732846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEpichlorohydrinHCID 7835—
ReactantDiethylene GlycolHCID 8117—
ReactantLanthanum perchlorate--water (1/3/6)HCID 44135853—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductDiethylene glycol monoglycidyl etherHCID 13640448—

Reaction Conditions

Temperature105 °C

Reaction Steps

Under a nitrogen atmosphere, 26.53 g of diethylene glycol, 0.25 g of lanthanum perchlorate hexahydrate and 50 ml of toluene are placed as the initial charge in a 350 ml sulfonating flask equipped with an intensive condenser and a propeller stirrer and heated to 105° C. After reaching an internal temperature of 105° C., with the temperature remaining constant 21.3 g of epichlorohydrin are added dropwise in the course of 70 minutes. After subsequently stirring for 14 hours at 105° C., 30 ml of toluene are added to the reaction mixture, in order then to remove by azeotropic distillation any water still present. At normal pressure about 30 ml of azeotrope are distilled off. After cooling to from 48 to 50° C., about 19 g of diazobicycloundecene are added dropwise in the course of 30 minutes and the mixture is subsequently stirred for 2 hours. After cooling to room temperature, the lower phase of the two-phase reaction mixture is adjusted to pH 5 to 8 using acetic acid, diluted with methylene chloride and extracted 3 times with approximately 100 ml of brine each time. After drying with magnesium sulfate, the crude product so obtained is concentrated to dryness and 27.1 g (73% of theory) of a slightly yellowish, viscous oil are obtained. 12 g of the crude product are purified by means of flash chromatography (800 g of silica gel 60 F; ethyl acetate 95: methanol 5). The desired product is obtained in the form of a slightly yellowish oil of approximately 85% purity (determined by GC). According to 1H-NMR spectrum, the by-product (15%, determined by GC) is the following compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07588880B2
Source datasetuspto-grants-2009_09
ORD IDord-3c996c283d47402eb3fd07f0f9a38cb0
Source noteuspto-grants-2009_09