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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874854Generated: November 5, 2026

1,2-Dichloroethane → HCID 59451364, compound

https://huagongshe.com/reaction/1874854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantIsobutyric AcidHCID 6590—
ReactantSodium CyanideHCID 8929—
ReactantAmmonium ChlorideHCID 25517—
Reactant(Phenylmethoxy)acetaldehydeHCID 108989—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
ProductHCID 59451364HCID 5945136465%

Reaction Steps

Benzyloxyacetaldehyde (1.5 g, 10.0 mmol) was added dropwise to a stirred solution of sodium cyanide (0.61 g, 12.4 mmol) and ammonium chloride (0.79 g, 14.8 mmol) in 25% ammonium hydroxide (5 mL). The solution was stirred at RT for 48 h, then extracted with CH2Cl2 (20 mL). The organic extract was washed with brine, dried (Na2SO4) and filtered. 2-Methylpropanoic acid (0.90 g, 10.2 mmol), EDC (2.85 g, 14.9 mmol) and DMAP (0.305 g, 2.5 mmol) were added to the filtrate and the solution was stirred for 12 h at RT. Water (10 mL) was added 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 (5-50% EtOAc:hexanes) to give the title compound (1.60 g, 65%) as an off-white solid. 1H NMR (400 MHz, CDCl3) δ ppm 7.31-7.44 (m, 5H), 6.13 (d, 1H), 5.06-5.13 (m, 1H), 4.64 (ABq, 2H), 3.69 (ABq, 2H), 2.32-2.45 (sept, 1H), 1.17 (t, 6H). ES-LCMS: m/z 247.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-71a3e571cd384929a229a79d85d00515
Source noteuspto-grants-2012_11