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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853148Generated: October 30, 2026

2-(4-benzyloxy-phenoxy)-N-methyl-acetamide → 2-(4-hydroxyphenoxy)-N-methylacetamide

https://huagongshe.com/reaction/853148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-benzyloxy-phenoxy)-N-methyl-acetamideHCID 11543606—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product2-(4-hydroxyphenoxy)-N-methylacetamideHCID 1818391394%

Reaction Steps

A solution of 4.7 g of 2-(4-benzyloxy-phenoxy)-N-methyl-acetamide [Example 2c)] in 150 ml of tetrahydrofurane was hydrogenated at atmospheric pressure and room temperature using 470 mg of palladium on charcoal (10%) as the catalyst. For the working-up, the reaction mixture was filtered over a Dicalite layer and the resulting solution was evaporated under reduced pressure. The residue was triturated in ether and the solid collected on a filter funnel. After drying there were obtained 2.95 g (93% of theory) of 2-(4-hydroxy-phenoxy)-N-methyl-acetamide as white crystals; MS: m/e=181 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253318B2
Source datasetuspto-grants-2007_08
ORD IDord-e192a3bf20ed42e99777025f1c54e5a5
Source noteuspto-grants-2007_08