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HRID 541004作成日:2026年10月26日

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

https://huagongshe.com/reaction/541004

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AzideHCID 33557—
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物Methyl S-benzyl-L-cysteinate hydrochlorideHCID 3084257—
反応物Methanesulfonyl azide, trifluoro-HCID 10986786—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-azido-3-(benzylsulfanyl)propanoateHCID 1418983875%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871916B2
出典データセットuspto-grants-2014_10
ORD IDord-54c085a0bdd947269e31ff86db81cb44
出典メモuspto-grants-2014_10