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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808722Generated: November 2, 2026

Ammonium Acetate → HCID 58353584, compound

https://huagongshe.com/reaction/1808722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 4-(2-oxopropyl)benzoateHCID 20134204—
SolventMethanolHCID 887—
ProductHCID 58353584HCID 5835358452%

Reaction Steps

Ethyl 4-(2-oxopropyl)benzoate (2.25 g, 10.9 mmol, 1 eq) and ammonium acetate (8.40 g, 109 mmol, 9.97 eq) were dissolved in MeOH (45 mL). While stirring at room temperature, sodium borohydride (684 mg, 18.1 mmol, 1.65 eq) was added. The resulting reaction mixture was stirred overnight at room temperature. The reaction was concentrated and partitioned between CH2Cl2 and 1M NaOH (aq.). The organic layer was removed and saved and the aqueous layer was extracted with CH2Cl2. The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, filtered, and evaporated to afford a residue which was purified via silica gel chromatography (gradient elution, 0% to 100% EtOAc in hexanes, SiO2) to afford ethyl 4-(2-hydroxypropyl)benzoate (1.18 g, 52%). The same silica gel column was then subjected to a second set of chromatography conditions (gradient elution, 0% to 80% MeOH in EtOAc) to afford racemic ethyl 4-(2-aminopropyl)benzoate (610 mg, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361959B2
Source datasetuspto-grants-2013_01
ORD IDord-52a22f1bd3af4fdba255ac2d44d47977
Source noteuspto-grants-2013_01