돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1761995생성일: 2026년 10월 24일

Sodium Hydroxide → 2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol 2-hydroxyethanesulfonate

https://huagongshe.com/ko/reaction/1761995

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Methanol--water (1/1)HCID 22242641—
반응물2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol methanesulfonateHCID 54096087—
생성물2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol 2-hydroxyethanesulfonateHCID 13171542270.4%

반응 단계

2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol methanesulfonate (1C, 10.0 g, 26.63 mmol) was neutralized with 1N NaOH (30 mL) in CH3OH/H2O (200/800 mL) as in procedure 1D. The white solid which formed was filtered, washed successively with warm H2O (3×500 mL), CH3OH (200 mL), and abs. Et2O (2×500 mL), sucked semi-dry and then resuspended in CH3OH (500 mL). To this was added a 0.43M aqueous solution of 2-hydroxyethanesulfonic acid (30 mL). Slight warming gave a solution which was then filtered. The solvent was removed by rotary evaporation to give a wet white solid. This was triturated with dry Et2O, filtered, and recrystallized 3× from EtOH/Et2O to give 8.8 g (70.4%) of 2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol 2-hydroxyethanesulfonate, mp 212°-213°, (C, H, N, S).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04829090
출처 데이터셋uspto-grants-1989_05
ORD IDord-8319c1b1b10a4798a5723e082b7f80df
출처 메모uspto-grants-1989_05