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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41074Generated: October 26, 2026

1,2-Dichloroethane → (R)-N-(2-hydroxy-1-phenylethyl)pent-4-enamide

https://huagongshe.com/reaction/41074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-Pentenoic acidHCID 61138—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant(R)-beta-aminophenethyl alcoholHCID 2724025—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product(R)-N-(2-hydroxy-1-phenylethyl)pent-4-enamideHCID 6731092664%

Reaction Steps

To a solution of 4-pentenoic acid (2.55 mL, 25.0 mmol) in DMF (312 mL) cooled in an ice/water bath was added HOBt (3.37 g, 25.0 mmol) and EDC (4.79 g, 25.0 mmol) and the resulting solution was stirred for 30 min (R)-(−)-2-phenylglycinol (3.43 g, 25.0 mmol), iPr2NEt (17.8 mL, 100 mmol), and DMAP (0.305 g, 2.50 mmol) were subsequently added and the reaction mixture was stirred 16 h at which point LC-MS analysis indicated complete consumption of starting material. The reaction mixture was diluted with saturated NH4Cl and EtOAc and the layers separated. The aqueous layer was extracted 2× with EtOAc and the combined organic extracts were washed with 1 N HCl and brine, dried over Na2SO4, filtered, and concentrated. The crude product was purified using silica gel chromatography (MeOH/CH2Cl2 gradient) to yield 3.5 g of product as a colorless oil in 64% yield. LRMS (M+H)+: 220.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530456B2
Source datasetuspto-grants-2013_09
ORD IDord-b71a08174352423d9dc2227546fe4c2a
Source noteuspto-grants-2013_09