1,4-Butanediol → HCID 23016554, compound

Temperature

60 °C

1,4-Butanediol (721 g (8.0 mol)) and toluene (350 ml) were added to a glass flask having an inner volume of 2,000 ml equipped with a stirrer, a thermometer, a dropping funnel and an reflux condenser, and mixture was warmed to 60° C. with stirring. Tetrabutylammonium bromide (38.7 g (0.12 mol)) and 96% sodium hydroxide (184 g (4.4 mol)) were added, and the mixture warmed to 75° C. with stirring. Subsequently 3-ethyl-3-methanesulfonyloxymethyloxetane (777 g (3.8 mol)) having purity of 95% synthesized by the same method as in Reference Example 1 was dropwise added while keeping a liquid temperature at 75-85° C., and the mixture was reacted at the same temperature for 2 hours. After the completion of the reaction, water (800 ml) was added to the reaction liquid (a bisoxetane ether compound generated in the amount of only 7% (an analysis value by a gas chromatography)), and a liquid separation was performed to give an organic layer. Toluene (800 ml) and water (400 ml) were added to a resultant organic layer, and acetic acid was added with stirring so that pH was adjusted to 9.5. After a liquid separation, an aqueous layer was extracted with toluene (400 ml) twice. An extract (a toluene layer) and an organic layer were combined, and the resultant was concentrated under reduced pressure. A resultant concentrate was distilled under reduced pressure (157-159° C., 1.9 kPa) to give, as a colorless liquid, 3-ethyl-3-(4-hydroxybutyl)oxymethyloxetane having a purity of 96% (an analysis value by a gas chromatography) (497 g) (an isolated yield based on 3-ethyl-3-methane-sulfonyloxymethyloxetane: 67%).

1. customequipped with a stirrer
2. temperaturethe mixture warmed to 75° C.
3. stirringwith stirring
4. customsynthesized by the same method as in Reference Example 1
5. additionwas dropwise added
6. customat 75-85° C.
7. customthe mixture was reacted at the same temperature for 2 hours
8. customa liquid separation
9. customto give an organic layer
10. additionwas added
11. stirringwith stirring so that pH
12. customAfter a liquid separation
13. extractionan aqueous layer was extracted with toluene (400 ml) twice
14. extractionAn extract (a toluene layer) and an organic layer
15. concentrationthe resultant was concentrated under reduced pressure
16. concentrationA resultant concentrate
17. distillationwas distilled under reduced pressure (157-159° C., 1.9 kPa)

ORD record

ord-fac3ddd9276d453a877dd4c611229bf6

Source dataset

uspto-grants-2012_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08247583B2