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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416150Generated: October 25, 2026

Acetic Acid → (S)-3-{[4-(3-fluorobenzyloxy)benzyl]methylamino}-pyrrolidin-2-one

https://huagongshe.com/reaction/1416150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantAcetonitrileHCID 6342—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(S)-3-[4-(3-fluorobenzyloxy) benzylamino]pyrrolidin-2-oneHCID 54532112—
Product(S)-3-{[4-(3-fluorobenzyloxy)benzyl]methylamino}-pyrrolidin-2-oneHCID 7006933170%

Reaction Steps

One g (0.00318 mol) of (S)-3-[4-(3-fluorobenzyloxy) benzylamino]pyrrolidin-2-one was dissolved in acetonitrile (50 ml) under a nitrogen stream. To this mixture, 1.6 ml (0.0196 mol) of 37% formaldehyde and 0.29 g (0.00460 mol) of sodium cyanoborohydride were added at room temperature. After 20 minutes, glacial acetic acid was dropped up to neutrality of the solution. The mixture was stirred for 40 minutes and was evaporated to dryness. 40 ml of 2 N KOH were added to the residue. After extracting with ethyl acetate, washing with N/2 KOH and then with water and brine, the organic layer was dried on Na2SO4, then filtered and evaporated to obtain a residue which was flash-chromatographed on silica gel (eluant: CHCl3 200: CH3OH 3: 30% NH4OH 0.2) to give 0.73 g (70%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912242
Source datasetuspto-grants-1999_06
ORD IDord-a23cda0c2e104bd6a74440c9764c1336
Source noteuspto-grants-1999_06