돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1386생성일: 2026년 10월 24일

Ethylene Glycol → 6-(2-methyl-1,3-dioxolan-2-yl)3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one

https://huagongshe.com/ko/reaction/1386

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물3,4-dihydro-4,4-dimethyl-6-acetyl-1(2H)-naphthalenoneHCID 11106782—
반응물3,4-dihydro-4,4-dimethyl-7-acetyl-1(2H)-naphthalenoneHCID 22323726—
용매BenzeneHCID 241—
생성물6-(2-methyl-1,3-dioxolan-2-yl)3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-oneHCID 15462843—

반응 단계

A solution of 1.80 g (8.34 mmol) of a 1:5 mixture of 3,4-dihydro-4,4-dimethyl-7-acetyl-naphthalen-1(2H)-one (Compound D14a); and 3,4-dihydro-4,4-dimethyl-6-acetyl-naphthalen-1(2H)-one (Compound D14b) in 50 mL benzene was combined with 517.7 mg (8.34 mmol) of ethylene glycol and 20.0 mg (0.11 mmol) of p-toluenesulfonic acid monohydrate. The resulting solution was heated to reflux for 18 h, cooled to room temperature, and concentrated under reduced pressure. The title compound was isolated by column chromatography (10% EtOAc-hexanes) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723666
출처 데이터셋uspto-grants-1998_03
ORD IDord-71d8a412e47743ae868fcc2cf8c525e8
출처 메모uspto-grants-1998_03