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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874867Generated: November 1, 2026

1,2-Dichloroethane → N-{1-cyano-2-[(phenylmethyl)oxy]ethyl}propanamide

https://huagongshe.com/reaction/1874867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantPropionic AcidHCID 1032—
ReactantSodium CyanideHCID 8929—
ReactantAmmonium ChlorideHCID 25517—
Reactant(Phenylmethoxy)acetaldehydeHCID 108989—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
ProductN-{1-cyano-2-[(phenylmethyl)oxy]ethyl}propanamideHCID 5945137578%

Reaction Steps

Benzyloxyacetaldehyde (3.0 g, 20.0 mmol) was added dropwise to a stirred solution of sodium cyanide (1.22 g, 24.9 mmol) and ammonium chloride (1.58 g, 29.5 mmol) in 25% ammonium hydroxide (9.6 mL). The solution was stirred at RT for 48 h, then extracted with CH2Cl2 (40 mL). The organic extract was washed with brine, dried (Na2SO4) and filtered. Propionic acid (1.5 g, 20.0 mmol), EDC (5.7 g, 30.0 mmol) and DMAP (610 mg, 5 mmol) were added to the filtrate and the solution was stirred for 12 h at RT. Water was added (20 mL) and the organic phase was separated and washed with 1N HCl (20 mL), dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel flash column chromatography (0-50% EtOAc:hexanes) to give the title compound (3.62 g, 78%) as a yellow oil. 1H NMR (400 MHz, CDCl3) δ ppm 7.32-7.43 (m, 5H), 6.09 (br. s., 1H), 5.08-5.13 (m, 1H), 4.59-4.69 (ABq, 2 H), 3.66 (ABq, 2H), 2.25 (qd, 2H), 1.17 (t, 3H). ES-LCMS: m/z 233.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-1f95db16b1694a4c8f977f0c21a2660e
Source noteuspto-grants-2012_11