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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915300Generated: October 26, 2026

Triphenylphosphine → N-[3-(3-methyl-but-3-enyloxy)-phenyl]-acetamide

https://huagongshe.com/reaction/1915300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-HydroxyacetanilideHCID 12124—
Reactant3-Methyl-3-buten-1-olHCID 12988—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantAcetic acid 3-formylamino-phenyl esterHCID 57470213—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductN-[3-(3-methyl-but-3-enyloxy)-phenyl]-acetamideHCID 5756738452%

Reaction Steps

A suspension of the mixture of N-(3-hydroxy-phenyl)-acetamide and acetic acid 3-formylamino-phenyl ester (18.12 g, 0.12 mol), 3-methyl-but-3-en-1-ol (8.6 g, 0.1 mol), DEAD (87 g, 0.2 mol) and Ph3P (31.44 g, 0.12 mol) in benzene (250 mL) was heated at reflux overnight and then cooled to room temperature. The reaction mixture was poured into water and the organic layer was separated. The aqueous phase was extracted with EtOAc (300×3 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated. The residue was purified by column chromatography to give N-[3-(3-methyl-but-3-enyloxy)-phenyl]-acetamide (11 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614327B2
Source datasetuspto-grants-2013_12
ORD IDord-e847831829eb4ac09f088219fec09df5
Source noteuspto-grants-2013_12