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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073407Generated: October 31, 2026

Ammonium Acetate → HCID 14552584, compound

https://huagongshe.com/reaction/1073407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 15662548HCID 15662548—
SolventMethanolHCID 887—
ProductHCID 14552584HCID 14552584—

Reaction Steps

Ammonium acetate (3.29 g, 42.7 mmol), sodium cyanoborohydride (0.20 g, 3.0 mmol) and 3A molecular sieves are added to the above phenoxyacetone (1.0 g, 4.3 mmol) in 20 ml of anhydrous methanol under N2 and at RT. The reaction is stirred at RT for 4 days. The methanol is removed by rotoevaporation, and ether and water are added to the residue, followed by 10% NaOH. The mixture is extracted with ether (3×), and the combined organic layers are washed with water until neutral, dried and filtered and the solvent evaporated off to give 2-[4-(3-methyl-2-butenoxy)phenoxy]-1-methylethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968829
Source datasetuspto-grants-1990_11
ORD IDord-5d5598bc2a4443b5b87c7d4ac1f473f2
Source noteuspto-grants-1990_11