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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59690Generated: October 26, 2026

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

https://huagongshe.com/reaction/59690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-beta-aminophenethyl alcoholHCID 2724025—
Reactant(+/-)-2,5-Dioxopyrrolidin-1-yl 2-methyl-5-phenylpentanoateHCID 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 numberUS09440919B2
Source datasetuspto-grants-2016_09
ORD IDord-845b5e6a71054bcaa8d4933eb583801c
Source noteuspto-grants-2016_09