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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162643Generated: October 29, 2026

(Bis(2-methoxyethyl)amino)sulfur trifluoride → (S)-3-azido-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1162643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
Reactanttrans-3-Azido-1-Boc-4-hydroxypyrrolidineHCID 11128048—
SolventDichloromethaneHCID 6344—
Product(S)-3-azido-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 8660883160.5%

Reaction Steps

37.1 To stirred, cooled (−78° C.) solution of 695 mg (3S,4S)-3-azido-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester (example 22.2) in 5 ml CH2Cl2 under an argon atmosphere were added 2.69 g bis(2-methoxyethyl)aminosulphur trifluoride (50% solution in THF). The dry ice bath was removed and the mixture was allowed to warm to r.t. and stirring was continued for 22 h. The mixture was poured into 10% aq. Na2CO3. The organic phase was washed with brine, dried (MgSO4), filtered and concentrated. The crude product was purified by chromatography (silica gel; gradient: cyclohexane->cyclohexane/EtOAc 3:2) to give 424 mg (S)-3-azido-4-fluoro-pyrrolidine-1-carboxylic acid tert-butyl ester as light yellow oil. MS 409.0 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820699B2
Source datasetuspto-grants-2010_10
ORD IDord-8d731baa95b54a3a9a9d499993623182
Source noteuspto-grants-2010_10