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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21557생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/21557

반응식

참여 물질

역할이름HCID투입량
반응물1-NaphthaldehydeHCID 6195—
반응물Diethyl MalonateHCID 7761—
반응물PiperidineHCID 8082—
용매BenzeneHCID 241—
생성물2-(1-Naphthylmethyl)-1,3-propanediolHCID 1403086690.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424309
출처 데이터셋uspto-grants-1995_06
ORD IDord-a6132d87997a4c09aa77677e86d88951
출처 메모uspto-grants-1995_06