1-Naphthaldehyde → 2-(1-Naphthylmethyl)-1,3-propanediol

2 g of 1-naphthoaldehyde, 2.3 g of diethyl malonate and 0.2 ml of piperidine were dissolved in 10 ml of benzene, and the solution was refluxed under heating for 6 hours while removing water by azeotropic distillation. The reaction solution was diluted with benzene, washed sequentially with 1N hydrochloric acid, with a saturated sodium hydrogencarbonate aqueous solution, with water and with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure. The residue was dissolved in a mixture consisting of 55 ml of ethanol and 37 ml of THF, and 2.7 g of sodium borohydride and 3.0 g of lithium chloride were added thereto under cooling with ice. The mixture was stirred at room temperature for 1 hour and then concentrated under reduced pressure. Water was added to the residue, and the solution was neutralized with 6N hydrochloric acid and extracted with ethyl acetate. The extract layer was washed with a saturated sodium hydrogencarbonate aqueous solution, with water and with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. Then, solvent was distilled off under reduced pressure. The residue was recrystallized from diethyl ether-n-hexane to obtain 2.5 g of 2-(1-naphthylmethyl)-1,3-propanediol.

1. temperaturethe solution was refluxed
2. temperatureunder heating for 6 hours
3. customwhile removing water
4. distillationby azeotropic distillation
5. additionThe reaction solution was diluted with benzene
6. washwashed sequentially with 1N hydrochloric acid, with a saturated sodium hydrogencarbonate aqueous solution, with water and with a saturated sodium chloride aqueous solution
7. dry with materialdried over anhydrous magnesium sulfate
8. distillationThen, the solvent was distilled off under reduced pressure
9. dissolutionThe residue was dissolved in a mixture
10. additionwere added
11. temperatureunder cooling with ice
12. concentrationconcentrated under reduced pressure
13. additionWater was added to the residue
14. extractionextracted with ethyl acetate
15. washThe extract layer was washed with a saturated sodium hydrogencarbonate aqueous solution, with water and with a saturated sodium chloride aqueous solution
16. dry with materialdried over anhydrous magnesium sulfate
17. distillationThen, solvent was distilled off under reduced pressure
18. customThe residue was recrystallized from diethyl ether-n-hexane

ORDレコード

ord-a6132d87997a4c09aa77677e86d88951

出典データセット

uspto-grants-1995_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05424309