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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2404147생성일: 2026년 10월 25일

Hydrochloric Acid → Methyl 1-((6-hydroxynaphthalen-2-yl)methyl)azetidine-3-carboxylate

https://huagongshe.com/reaction/2404147

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 1-((6-(tert-butyldimethylsilyloxy)naphthalen-2-yl)methyl)azetidine-3-carboxylateHCID 66926610—
용매MethanolHCID 887—
생성물Methyl 1-((6-hydroxynaphthalen-2-yl)methyl)azetidine-3-carboxylateHCID 6692593447.3%

반응 단계

To a solution of methyl 1-((6-(tert-butyldimethylsilyloxy)naphthalen-2-yl)methyl)azetidine-3-carboxylate (4.5 g, 11.7 mmol) in methanol (50 mL) at 0° C. was added con. HCl (5 mL) dropwise. The reaction mixture was stirred at r.t for 1 h. The mixture was neutralized by sat. NaHCO3 and evaporated off most of solvent, extracted with DCM and washed with brine, dried over Na2SO4 and concentrated to obtain crude product. The crude product was purified by silica gel chromatography (DCM:MeOH=40:1), extracted with DCM and washed with brine, dried over Na2SO4 and concentrated to obtain crude product. The crude product was purified by silica gel chromatography (DCM:MeOH=40:1) to give the title compound (1.5 g, 47%) as a gray solid. ESI-MS (M+1)+: 272.0. 1H NMR (400 MHz, CDCl3) δ: 8.14 (s, 1H), 7.59-7.52 (m, 2H), 7.39-7.28 (m, 2H), 7.09-7.04 (m, 2H), 3.92 (s, 2H), 3.86-3.82 (m, 2H), 3.70 (s, 3H), 3.63-3.59 (m, 2H), 3.52-3.46 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08802659B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-d368c7d099e44e71b33cb7d62227a397
출처 메모uspto-grants-2014_08