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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 541004Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/541004

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium AzideHCID 33557—
EduktTrifluoromethanesulfonic anhydrideHCID 67749—
EduktMethyl S-benzyl-L-cysteinate hydrochlorideHCID 3084257—
EduktMethanesulfonyl azide, trifluoro-HCID 10986786—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 2-azido-3-(benzylsulfanyl)propanoateHCID 1418983875%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08871916B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-54c085a0bdd947269e31ff86db81cb44
Quellennotizuspto-grants-2014_10