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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804960Generated: October 26, 2026

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

https://huagongshe.com/reaction/1804960

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 numberUS08354427B2
Source datasetuspto-grants-2013_01
ORD IDord-f0eaae2deb4840b2be23245cc1a6def4
Source noteuspto-grants-2013_01