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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709103Generated: October 25, 2026

(R)-beta-aminophenethyl alcohol → (5)-N-((R)-2-hydroxy-1-phenylethyl)-2-methyl-5-phenylpentanamide

https://huagongshe.com/reaction/709103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-beta-aminophenethyl alcoholHCID 2724025—
ReactantHCID 90026070HCID 90026070—
SolventTetrahydrofuranHCID 8028—
Product(5)-N-((R)-2-hydroxy-1-phenylethyl)-2-methyl-5-phenylpentanamideHCID 9002582434%

Reaction Conditions

Temperature48 °C

Reaction Steps

To a solution consisting of (±)-2,5-dioxopyrrolidin-1-yl 2-methyl-5-phenyl pentanoate (18mb(i), 85.6 g, 296 mmol) in THF (3000 mL) at 48° C. was added R-(−)-2-phenylglycinol (65.9 g, 480 mmol, Bridge Organics) in portions. The resulting reaction mixture was stirred at 48° C. for 40 hours. A white precipitate formed, which was filtered from the reaction mixture and washed with THF. The filtrate was concentrated under vacuum and the residue, comprising the diastereomeric pair, was chromatographed on silica gel. Elution with ethyl acetate-heptane (50:50 v/v) afforded the pure diastereomer title compound (31.3 g, 34%) as a colorless solid; TLC Rf 0.205 (solvent system: 50:50 v/v ethyl acetate-heptane); HPLC retention time 15.1 minutes, stationary phase: Gemini 5μ C18 250×4.6 mm, ultraviolet detector at 210 nm, mobile phase: 1 mL/min, 60:40:0.1 v/v methanol-water-acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180116B2
Source datasetuspto-grants-2015_11
ORD IDord-69bff5405f684703a9a4bc9e8ea90662
Source noteuspto-grants-2015_11