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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508155Generated: October 30, 2026

Ethyl Acetate → HCID 178424503, compound

https://huagongshe.com/reaction/1508155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-Butanaminium, N,N,N-tributyl-, fluoride, hydrateHCID 16211673—
ReactantHCID 58994328HCID 58994328—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178424503HCID 17842450392%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid [4-[2-(tert-butyl-dimethyl-silanyloxy)-1,1-dimethyl-ethyl]-2-(4,4-dimethyl-cyclohex-1-enyl)-phenyl]-amide (as prepared in the previous step, 2.20 g, 3.45 mmol) and tetrabutylammonium fluoride hydrate (4.52 g, 17.3 mmol) in 25 mL of THF was stirred at 50° C. for 3 h. After cooling to RT, the mixture was treated with 100 mL of EtOAc and washed with saturated aqueous NH4Cl (20 mL), H2O (20 mL) and brine (20 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel chromatography (0-4% MeOH/DCM) to afford the title compound (1.25 g, 92%) as a white solid. Mass spectrum (ESI, m/z): Calcd. for C23H28N4O2, 393.2 (M+H). found 393.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221797B2
Source datasetuspto-grants-2015_12
ORD IDord-817e28013cd843c7aceb98716e3172a5
Source noteuspto-grants-2015_12