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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902344Generated: October 30, 2026

Triphenylphosphine → HCID 24878193, compound

https://huagongshe.com/reaction/902344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 86609132HCID 86609132—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 24878193HCID 24878193—

Reaction Steps

To a solution of (R)-2-(azidomethyl)-9-(2,6-dichlorophenyl)-7-fluoro-2,3,4,5-tetrahydrobenzo[b]oxepine (0.17 g, 0.46 mmol) in tetrahydrofuran (10 mL) and water (1 mL) was added polymer-bound triphenylphosphine (˜3 mmol/g, 0.46 g, 1.4 mmol) and the reaction mixture stirred at room temperature for 2 days. The brown suspension was then filtered through celite, the filter cake washed with ethyl acetate (50 mL) and the combined filtrates concentrated under vacuum. The solvent was removed under vacuum. Chromatography with 0–10% methanol in methylene chloride plus 1% NH4OH afforded {[(R)-8-(2,6-dichlorophenyl)-6-fluoro-3,4-dihydro-2H-chromen-2-yl]methyl}amine as a colorless oil. The colorless oil was dissolved in ethyl acetate and made into its hydrochloride salt (0.13 g, 71%) as a white foam using excess ethereal hydrochloric acid, [α]D25=+38.22° (c 1% solution in MeOH); MS (ES) m/z 340.0 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365095B2
Source datasetuspto-grants-2008_04
ORD IDord-05e7e2aad9094a0a9b30b060275ea01a
Source noteuspto-grants-2008_04