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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039952Generated: October 31, 2026

Sodium Azide → (3R,5S)-5-(azidomethyl)-3-(3-chloropropyl)pyrrolidin-2-one

https://huagongshe.com/reaction/2039952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantAzideHCID 33558—
Reactant((2S,4R)-4-(3-chloropropyl)-5-oxopyrrolidin-2-yl)methyl 4-nitrobenzenesulfonateHCID 58011487—
SolventDimethylformamideHCID 6228—
Product(3R,5S)-5-(azidomethyl)-3-(3-chloropropyl)pyrrolidin-2-oneHCID 86637155—

Reaction Steps

The ((2S,4R)-4-(3-chloropropyl)-5-oxopyrrolidin-2-yl)methyl 4-nitrobenzenesulfonate (18.05 g, 45.2 mmol) and NaN3 (3.23 g, 49.7 mmol, 1.1 equiv) were stirred in 100 mL of DMF for 19 h. After this time a white solid had formed and LC/MS analysis showed formation of the desired azide. The DMF was removed in vacuo and the residue partitioned between EtOAc/H2O (100+100 mL). The mixture was transferred to a separatory funnel and the layers separated. The aqueous layer was extracted with 100 mL additional EtOAc and the combined organic extracts washed with brine, dried over Na2SO4, filtered and evaporated. The (3R,5S)-5-(azidomethyl)-3-(3-chloropropyl)pyrrolidin-2-one was isolated as a pale yellow syrup (9.08 g, 94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580823B2
Source datasetuspto-grants-2013_11
ORD IDord-00c371c89e4f46b69828f92f9a0836f4
Source noteuspto-grants-2013_11