Toluene → Diethylene glycol monoglycidyl ether

온도

105 °C

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:

1. additioninitial charge in a 350 ml
2. customequipped with an intensive condenser and a propeller stirrer
3. customan internal temperature of 105° C.
4. additionare added dropwise in the course of 70 minutes
5. customto remove by azeotropic distillation any water still present
6. distillationAt normal pressure about 30 ml of azeotrope are distilled off
7. temperatureAfter cooling to from 48 to 50° C., about 19 g of diazobicycloundecene
8. additionare added dropwise in the course of 30 minutes
9. stirringthe mixture is subsequently stirred for 2 hours
10. temperatureAfter cooling to room temperature
11. customthe lower phase of the two-phase reaction mixture
12. extractionextracted 3 times with approximately 100 ml of brine each time
13. dry with materialAfter drying with magnesium sulfate
14. customthe crude product so obtained
15. concentrationis concentrated to dryness and 27.1 g (73% of theory) of a slightly yellowish, viscous oil
16. customare obtained
17. custom12 g of the crude product are purified by means of flash chromatography (800 g of silica gel 60 F; ethyl acetate 95: methanol 5)

ORD 기록

ord-3c996c283d47402eb3fd07f0f9a38cb0

출처 데이터셋

uspto-grants-2009_09

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07588880B2