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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632468Generated: November 3, 2026

Triphenylphosphine → HCID 20442920, compound

https://huagongshe.com/reaction/1632468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 13366425HCID 13366425—
SolventAcetonitrileHCID 6342—
ProductHCID 20442920HCID 20442920—

Reaction Steps

The crude (4-trifluoromethoxy-2,3,6-trimethylphenyl)methyl chloride, 27.5 g (0.104 mol) of triphenylphosphine and 250 ml of acetonitrile were heated to reflux for 20 hours. The solvent was removed on a rotary evaporator at room temperature and the residue was triturated with 300 ml of ethyl acetate. The resulting solid was filtered, dissolved in 250 ml of hot acetonitrile and treated with 1 liter of ethyl acetate. The mixture was allowed to stand 2 hours; 38 g of (4-trifluoromethoxy-2,3,6-trimethylphenyl)methyltriphenylphosphonium chloride was collected; mp 272°-274° C. In a similar manner, the mother liquor afforded an additional 10.5 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04476056
Source datasetuspto-grants-1984_10
ORD IDord-0a9c9d9bc8964b4594050950d017acd8
Source noteuspto-grants-1984_10