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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 541004생성일: 2026년 10월 26일

Sodium Azide → Methyl 2-azido-3-(benzylsulfanyl)propanoate

https://huagongshe.com/reaction/541004

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AzideHCID 33557—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물Methyl S-benzyl-L-cysteinate hydrochlorideHCID 3084257—
반응물Methanesulfonyl azide, trifluoro-HCID 10986786—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Methyl 2-azido-3-(benzylsulfanyl)propanoateHCID 1418983875%

반응 단계

Following a method described by Aubé and coworkers [S. K. Ramanathan, J. Keeler, H.-L. Lee, D. S. Reddy, G. Lushington, J. Aubé, Org. Lett. 2005, 7, 1059-1062], a solution of NaN3 (0.88 g, 13.7 mmol) in H2O (2.5 mL) was cooled to 0° C. and CH2Cl2 (4 mL) was added. Whilst the mixture was stirring vigorously, Tf2O (CF3SO2OSO2CF3, 0.47 mL, 2.26 mmol) was added dropwise. The resulting solution was stirred for an additional 2 h. The mixture was then placed in a separating funnel, and the organic layer was removed. The aqueous phase was extracted further with CH2Cl2 (2×3 mL). The organic layers were combined, washed with saturated Na2CO3, dried over Na2SO4(s), and filtered. The resulting solution of TfN3 was added dropwise to a solution of methyl 2-amino-3-(benzylsulfanyl)propanoate hydrochloride salt (0.37 g, 1.40 mmol) and DMAP (0.75 g, 6.16 mmol) in CH2Cl2 (5 mL). The resulting solution was stirred overnight under Ar(g). The mixture was concentrated under reduced pressure and purified by silica gel flash chromatography, eluting with CH2Cl2, to give azide 2e as an oil (0.26 g, 1.05 mmol, 75% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871916B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-54c085a0bdd947269e31ff86db81cb44
출처 메모uspto-grants-2014_10