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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253146생성일: 2026년 10월 24일

Water → Benzyl 4-(2-(4-propyl-1H-1,2,3-triazol-1-yl)acetyl)morpholine-2-carboxylate

https://huagongshe.com/ko/reaction/253146

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-PentyneHCID 12309—
반응물Sodium AscorbateHCID 23667548—
반응물Benzyl 4-(2-azidoacetyl)morpholine-2-carboxylateHCID 86614022—
촉매Copper sulfate pentahydrateHCID 24463—
용매tert-ButanolHCID 6386—
용매Ethyl AcetateHCID 8857—
생성물Benzyl 4-(2-(4-propyl-1H-1,2,3-triazol-1-yl)acetyl)morpholine-2-carboxylateHCID 66845266875%

반응 단계

In a sealable vessel, benzyl 4-(2-azidoacetyl)morpholine-2-carboxylate (0.096 g, 0.32 mmol) was suspended in t-BuOH (1 mL) and water (1 mL) was added. An aqueous solution of sodium ascorbate (1.0 M, 0.032 ml, 0.032 mmol) and an aqueous solution of copper(II) sulfate pentahydrate (0.30 M, 0.079 ml, 0.024 mmol) were added, followed by pent-1-yne (0.040 ml, 0.41 mmol). The vessel was sealed and placed in a 65 deg oil bath, whereupon the mixture was stirred for 14 h. The reaction mixture was cooled to RT, taken up in EtOAc (60 mL), and the organic layer was extracted with dilute sodium bicarbonate (5 mL), dilute brine (5 mL), and saturated brine (5 mL), then was dried over sodium sulfate and concentrated. The residue was purified through silica gel (25 mL) eluting with EtOAc, affording the title compound (105 mg, 0.28 mmol). MS m/z 373 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872009B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-faeb4f8a57de4cb992633bfb8d63a567
출처 메모uspto-grants-2011_01