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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676863Generated: October 30, 2026

Acetic Anhydride → HCID 58786333, compound

https://huagongshe.com/reaction/1676863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(1,3-benzodioxol-5-yl)-N-(1,3-benzodioxol-5-ylmethyl)-N-[(1-butyl-4-phenyl-1H-imidazol-5-yl)methyl]methanamineHCID 67370933—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58786333HCID 58786333—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-BuLi (1.2 equivalents in 175 μl hexane) is added to a solution of 1-(1,3-benzodioxol-5-yl)-N-(1,3-benzodioxol-5-ylmethyl)-N-[(1-butyl-4-phenyl-1H-imidazol-5-yl)methyl]methanamine (118 mg), obtained as a minor product in Example 2, step 4, in 10 mL anhydrous THF under N2 at −78° C. The resulting mixture is stirred at −78° C. for 1 hour. Ac2O (118.4 mg, 1.2 equivalents) is added. The reaction mixture is stirred at −78° C. for 2 more hours, warned to room temperature, and stirred overnight. The reaction is quenched with 5 mL of H2O and diluted with 20 mL ethyl acetate. The organic phase is collected, washed with brine, dried and concentrated. Purification via silica gel chromatography provides the title compound (Compound 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08007767B2
Source datasetuspto-grants-2011_08
ORD IDord-190d014bb15744dca77e0e3cca7fbcb0
Source noteuspto-grants-2011_08