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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726932Generated: November 2, 2026

Ethyl Acetate → HCID 178448753, compound

https://huagongshe.com/reaction/1726932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 68963075HCID 68963075—
ReactantHCID 178418370HCID 178418370—
SolventDiethyl EtherHCID 3283—
ProductHCID 178448753HCID 17844875386%

Reaction Steps

4-Methylphenylmagnesium bromide (1.64 mL, 1.0 M in ether) was added all at once via syringe to a well-stirred solution of 1-n-butyl-3-methyl-1,2,4-triazin-6-one (178 mg, 1.06 mmol) in ether (9.85 mL) under N2 at room temperature. After stirring the resulting mixture overnight, saturated aqueous NH4Cl (10 mL) and ethyl acetate (10 mL) were added, the organic phase was separated, and the aqueous layer was extracted once more with ethyl acetate. The combined organic layers were dried over Na2SO4 and evaporated to dryness. The crude product was purified by flash chromatography on silica gel (5 g, 4:1 hexanes:ethyl acetate) to afford Compound 22 as a tan solid (236 mg, 86% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494996B2
Source datasetuspto-grants-2009_02
ORD IDord-dbfd02af5abf4944aad8f9d3426084dd
Source noteuspto-grants-2009_02