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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606781생성일: 2026년 10월 27일

Triglyme → 3-(p-Chlorophenethyl)-8-oxa-3-azabicyclo(3.2.1)octane

https://huagongshe.com/reaction/1606781

반응식

참여 물질

역할이름HCID투입량
반응물TriglymeHCID 8189—
반응물Sodium HydroxideHCID 14798—
반응물2-(4-Chlorophenyl)ethylamineHCID 67430—
반응물(Tetrahydrofuran-2,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate)HCID 259634—
생성물3-(p-Chlorophenethyl)-8-oxa-3-azabicyclo(3.2.1)octaneHCID 21544555—

반응 조건

온도180 °C

반응 단계

p-Chlorophenethylamine (0.643 mole, 100 grams) was added to a mixture of 2,5-bis(tosyloxymethyl)tetrahydrofuran (0.214 mole, 99.6 grams) and 200 ml of Ansul 161 (triethylene glycol dimethyl ether) and stirred the reaction mixture for 3 hours at 180° C. The reaction mixture was cooled to room temperature and neutralized with a methanolic sodium hydroxide solution (0.429 mole, 17.14 grams NaOH in 200 ml CH3OH) while stirring for 15 minutes. The solvents and excess starting amine were distilled from the reaction mixture under aspirator pressure. The residue was filtered collecting the sodium p-toluenesulfonate. The filtrate was distilled collecting one fraction (terminal pot temperature 280° C./0.1 mm Hg). The distillate which solidified was recrystallized from methanol obtaining 3-(p-chlorophenethyl)-8-oxa-3-azabicyclo(3.2.1)octane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03953596
출처 데이터셋uspto-grants-1976_04
ORD IDord-d58de6d27fe040538899deb8fcb4ce27
출처 메모uspto-grants-1976_04