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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589940Generated: October 30, 2026

Ammonia → HCID 117701134, compound

https://huagongshe.com/reaction/589940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantButanoic acid, 2-bromo-, ethyl esterHCID 79039—
Reactant4-cyclopropanecarbonylphenolHCID 1051512—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117701134HCID 11770113487.6%

Reaction Steps

Tripotassium phosphate (8.17 g, 38.5 mmol) and ethyl 2-bromobutyrate (4.77 mL, 32.6 mmol) were added to an acetone (24 mL) solution of cyclopropyl(4-hydroxyphenyl)methanone (4.80 g, 29.6 mmol) at room temperature, and the mixture was stirred for 4 hours under reflux. Tripotassium phosphate (1.57 g, 7.40 mmol) and ethyl 2-bromobutyrate (1.08 mL, 7.40 mmol) were added to the mixture at room temperature, and the resulting mixture was stirred for 3 hours under reflux. After the reaction mixture was cooled to room temperature, water was added to the reaction mixture, and the resulting mixture was extracted once with acetone. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1→1:1, v/v). Subsequently, the compound thus obtained was dissolved in water (45 mL), then 5 M aqueous sodium hydroxide solution (8.78 mL, 44.4 mmol) was added to the mixture at room temperature, and the resulting mixture was stirred at the same temperature for 2 hours. Water and a saturated aqueous solution of ammonium chloride were added to the reaction mixture, and the mixture was extracted three times with ethyl acetate, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. Carbonyldiimidazole (7.20 g, 44.4 mmol) was added to a tetrahydrofuran (150 mL) solution of the compound thus obtained (7.35 g, 29.5 mmol) at room temperature, and the mixture was stirred at the same temperature for 30 minutes. A 28% aqueous ammonia solution (30 mL, excess amount) was added to the mixture at room temperature, and the resulting mixture was stirred at the same temperature for 30 minutes. Water was added to the reaction mixture, and the resulting mixture was extracted three times with ethyl acetate, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1→ethyl acetate, v/v) to give the title compound (6.41 g, yield: 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233958B2
Source datasetuspto-grants-2016_01
ORD IDord-d5d7e659e3634c93ba831a7ca89aebbf
Source noteuspto-grants-2016_01