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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161440Generated: October 29, 2026

Triphenylphosphine → 5-Fluoro-8-methoxychromane

https://huagongshe.com/reaction/1161440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant3-Fluoro-2-(3-hydroxypropyl)-6-methoxyphenolHCID 59511911—
SolventTetrahydrofuranHCID 8028—
Product5-Fluoro-8-methoxychromaneHCID 5951181482.8%

Reaction Conditions

Temperature-74 °C

Reaction Steps

After dissolving 4.78 g of 3-fluoro-2-(3-hydroxypropyl)-6-methoxyphenol and 9.4 g of triphenylphosphine in 70 ml of THF under a nitrogen atmosphere, the solution was cooled to −74° C. Next, 7 ml of DIAD was added to the reaction mixture, and the temperature was allowed to rise to room temperature prior to stirring overnight. The reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (3.6 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-f597a51b1f4745179847006cdc257073
Source noteuspto-grants-2010_10