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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196834Generated: November 1, 2026

Phenethylamine → (2S,3R)-3-(3-Phenethylamino-propyl)-1-((S)-1-phenyl-ethyl)-pyrrolidine-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2196834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(2S,3R)-1-((2E,4Z)-(S)-1,2-Dimethyl-hexa-2,4-dienyl)-3-(3-oxo-propyl) pyrrolidine-2-carboxylic acid ethyl esterHCID 86601083—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product(2S,3R)-3-(3-Phenethylamino-propyl)-1-((S)-1-phenyl-ethyl)-pyrrolidine-2-carboxylic acid ethyl esterHCID 6700417030.5%

Reaction Steps

To a solution of (2S,3R)-1-((2E,4Z)—(S)-1,2-Dimethyl-hexa-2,4-dienyl)-3-(3-oxo-propyl)pyrrolidine-2-carboxylic acid ethyl ester (1 g, crude) in EtOH (10 mL) is added phenethylamine (0.44 g, 3.65 mmol) at r.t. After stirring at r.t. for 30 min, NaBH3CN (0.3 g, 4.87 mmol) is added in one portion, After stirring at r.t. for 1.5 Hrs, the reaction solution is diluted with 50 mL of ether and washed with 20 mL of brine. The ether layer is concentrated and the crude product is purified by chromatography (CH2Cl2/MeOH: 97/3) to give a pale liquid (405 mg, 30.0%). (NMR and MS data confirmed, U-4117-52-20).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338440B2
Source datasetuspto-grants-2012_12
ORD IDord-b84812c800224adeb8fa847a8041cabe
Source noteuspto-grants-2012_12