Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272194Generated: November 2, 2026

Ammonium Acetate → HCID 22723464, compound

https://huagongshe.com/reaction/1272194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium FormateHCID 2723810—
Reactant1-[2-(Benzyloxy)phenyl]-2-bromoethan-1-oneHCID 12541850—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22723464HCID 2272346424.2%

Reaction Steps

A mixture of 2-bromo-1-(2-benzyloxyphenyl)ethanone (J. Med. Chem., 35:3045, 1992; 10.0 g, 32.77 mmol) and sodium formate (4.46 g, 65.6 mmol) in dry dimethylformamide (100 ml) is stirred at room temperature overnight. The mixture is poured into water (400 ml) and extracted with dichloromethane (2×100 ml). The combined extracts are dried over sodium sulfate and concentrated under reduced pressure. The residue is dissolved in acetic acid (100 ml), treated with ammonium acetate (12.62 g, 163.7 mmol), and the mixture is heated for 3 hours. After cooling, the mixture is diluted with water (400 ml) and extracted with dichloromethane (2×100 ml). The combined organic layers are washed with saturated aqueous sodium bicarbonate solution (2×100 ml), dried over sodium sulfate, and concentrated in vacuo. 4-(2-Benzyloxyphenyl)oxazole (1.99 g, 24%) is obtained after chromatography (silica gel, dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208505B2
Source datasetuspto-grants-2007_04
ORD IDord-1a97bb534e7e40279eb7ea4052ada2b7
Source noteuspto-grants-2007_04