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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218437Generated: October 30, 2026

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

https://huagongshe.com/reaction/218437

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 numberUS08198453B2
Source datasetuspto-grants-2012_06
ORD IDord-4cf8c6d931fb445c88b74b0b9ee57cf9
Source noteuspto-grants-2012_06