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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1078976생성일: 2026년 10월 26일

3,4-Dihydroisoquinoline → N-(n-Octyl)-3,4-Dihydroisoquinoline p-toluenesulfonate

https://huagongshe.com/reaction/1078976

반응식

참여 물질

역할이름HCID투입량
반응물3,4-DihydroisoquinolineHCID 76705—
반응물n-Octyl p-ToluenesulfonateHCID 599296—
용매MethanolHCID 887—
생성물N-(n-Octyl)-3,4-Dihydroisoquinoline p-toluenesulfonateHCID 231946667.4%

반응 단계

3,4-Dihydroisoquinoline (1.31 g, 10.0 mmol) was dissolved in 3 ml MeOH in a 3-neck 25 ml round bottom flask fitted with a condenser, drying tube and stirrer bar, and cooled in an ice bath. n-Octyl p-toluenesulfonate (2.84g, 10.0 mmol)*, dissolved in 7.0 ml methanol, was added dropwise over about 7 minutes via an addition funnel. The ice bath was removed and replaced with an oil bath and the colorless clear solution heated to reflux for at least 8 hours during which time the reaction solution turned yellow. Removal of the methanol in vacuo gave slightly colored solid product which was triturated with about 7.5 ml acetone. The acetone insoluble solids were filtered, washed with more acetone and dried in a vacuum desiccator. Yield of colorless solids was 1.91 g. A second batch of solids was recovered from the acetone filtrate/washing and filtered, washed with acetone and dried to give 0.31 gm colorless solids.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05550256
출처 데이터셋uspto-grants-1996_08
ORD IDord-7cf6bddd79694753879e7bb235170743
출처 메모uspto-grants-1996_08