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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75178Generated: October 28, 2026

Potassium Carbonate → (3-Cyano-3-butene-1-yl)(ethoxycarbonyl)azanyl 1,1-dimethylethyl carbonate

https://huagongshe.com/reaction/75178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methylsulfonyloxy-2-(hydroxymethyl) butanenitrileHCID 86674470—
Reactant1,1-Dimethylethyl (ethoxycarbonyl)azanyl carbonateHCID 86674471—
Reactant1,1-Dimethylethyl(ethoxycarbonyl)azanyl carbonateHCID 86674472—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(3-Cyano-3-butene-1-yl)(ethoxycarbonyl)azanyl 1,1-dimethylethyl carbonateHCID 86674469—

Reaction Steps

A mixture of 4-methylsulfonyloxy-2-(hydroxymethyl) butanenitrile (i.e. the product of Step E) (6.87 g, 0.039 mol), 1,1-dimethylethyl (ethoxycarbonyl)azanyl carbonate (7.65 g, 0.037 mol) (i.e. the product of Step F) and potassium carbonate (10.21 g, 0.074 mol) in N,N-dimethylformamide (50 mL) was stirred at room temperature for 20 h. The reaction mixture was poured onto iced water (100 mL) and extracted with diethyl ether (3×50 mL). The combined organic layers were washed with water (50 mL) and concentrated to a pale-tan oil (10.05 g). The oil was adsorbed onto Celite® (diatomaceous filter aid), and then purified by silica gel chromatography (0-100% gradient of ethyl acetate in petroleum ether as eluant). The appropriate fractions were combined to provide the title compound as a yellow oil (3.78 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835427B2
Source datasetuspto-grants-2014_09
ORD IDord-b33f2e5e72ee4041adbf8b4167d0f42f
Source noteuspto-grants-2014_09