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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638971Generated: October 30, 2026

Acetonitrile → HCID 178487887, compound

https://huagongshe.com/reaction/638971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantIsopropanol carbon dioxideHCID 86586944—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178498551HCID 178498551—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178487887HCID 17848788785%

Reaction Conditions

Temperature-72 °C

Reaction Steps

To a cold solution of acetonitrile (2 mL, 38 mmol, 2.8 eq) in THF (30 mL) at −72° C. (Dry-ice/IPA) was added dropwise nBuLi (12 mL, 30 mmol, 2.2 eq) under argon atmosphere. The reaction mixture became an orange suspension after 1 h. A solution of methyl 2-{[(1E)-(dimethylamino)methylidene]amino}-5-(methyloxy)benzoate (3.2 g, 13.6 mmol, 1 eq) in THF (30 mL) was then added dropwise while the internal temperature was maintained at −72° C. The resulting mixture was slowly warmed to RT overnight. To the resulting light-brown suspension was added glacial acetic acid (6 mL) with slight cooling. After stirring for 1 h, the suspension was then quenched with water (60 mL) and filtered to give the titled compound (2.3 g, 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691850B2
Source datasetuspto-grants-2010_04
ORD IDord-94978249b62c40058da8e719f6de3ca8
Source noteuspto-grants-2010_04