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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676963Generated: October 30, 2026

(S)-(+)-1-(2-Pyrrolidinylmethyl)pyrrolidine → Pyrrolidine, 1-(4-bromobenzoyl)-2-(1-pyrrolidinylmethyl)-, (2S)-

https://huagongshe.com/reaction/1676963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-1-(2-Pyrrolidinylmethyl)pyrrolidineHCID 853152—
Reactant2,5-Dioxopyrrolidin-1-yl 4-bromobenzoateHCID 13896430—
SolventTetrahydrofuranHCID 8028—
ProductPyrrolidine, 1-(4-bromobenzoyl)-2-(1-pyrrolidinylmethyl)-, (2S)-HCID 1196512971%

Reaction Steps

To a stirring solution of 4-bromobenzoic acid-2,5-dioxo-pyrrolidin-1-yl ester (3.5 g, 11.7 mmol) [CAS: 80586-82-9] in tetrahydrofuran (0.15M), is added (S)-(+)-1-(2-pyrrolidinylmethyl)pyrrolidine (1.9 mL, 11.7 mmol) and the mixture heated to reflux for 4 h. The reaction is allowed to cool to room temperature and washed with water while extracting with 10% isopropanol/dichloromethane. The organic portion is dried with sodium sulfate, filtered; and concentrated in vacuo. The resulting residue is purified on a silica gel column, eluting with 2M ammonia in methanol and dichloromethane to obtain 2.80 g (71%) of the title compound. MS (ES+) m/e 337.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008296B2
Source datasetuspto-grants-2011_08
ORD IDord-c261f1a3fe5740a2bbccad98eea0452e
Source noteuspto-grants-2011_08