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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210072Generated: October 30, 2026

O-Xylene → 7-(phenylmethoxy)-8-(2-propenyl)-4H-1-benzopyran-4-one

https://huagongshe.com/reaction/2210072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant1-[2-Hydroxy-4-(phenylmethoxy)-3-(2-propenyl)phenyl]ethanoneHCID 15048041—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product7-(phenylmethoxy)-8-(2-propenyl)-4H-1-benzopyran-4-oneHCID 1937993067.6%

Reaction Steps

A mixture of 5.0 g (17.73 mmol) of 1-[2-hydroxy-4-(phenylmethoxy)-3-(2-propenyl)phenyl]ethanone, 2.3 g (19.48 mmol) of dimethylformamide dimethyl acetal, and 5.0 mL of xylene was stirred and heated in a 120°-130° C. oil-bath as methanol was distilled out using a 3 in. Vigreux column, over a 2.5 hr period. The bath temperature was then raised to 150°-160° C. and the reaction mixture was stirred at this temperature for an additional 30 min. The mixture was cooled and concentrated at 60° C./high vacuum. To the viscous, red-brown, oily residue was added 3.7 g (19.48 mmol) of p-toluenesulfonic acid monohydrate and 50 mL of ethanol. The resulting solution was stirred and refluxed for 24 hr, then cooled and diluted with water. Work-up with ether in the usual manner gave a crude product which was recrystallized from hexane-ethyl acetate. There was obtained 3.5 g (67.6%) of 7-(phenylmethoxy)-8-(2-propenyl)-4H-1-benzopyran-4-one as a yellow solid, mp 90°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457124
Source datasetuspto-grants-1995_10
ORD IDord-9b0c91652c9e4e7784496719dd9f3b57
Source noteuspto-grants-1995_10