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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382918Generated: November 1, 2026

Triphenylphosphine → HCID 21273347, compound

https://huagongshe.com/reaction/1382918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 13983022HCID 13983022—
SolventTolueneHCID 1140—
ProductHCID 21273347HCID 2127334735.4%

Reaction Steps

A mixture of 7.25 g (28.4 mmole) of 6-bromomethyl-4,4-dimethylchroman, 14.8 g (56.8 mmole) of triphenylphosphine and 100 ml of toluene were heated under reflux for 12 hours, and then the solvent was removed by evaporation in vacuo. The residue (an oil) was dissolved in dichloromethane and decolorized with activated carbon. The solvent was removed by evaporation in vacuo and the residue was triturated under hexane to remove starting materials. The product so obtained was recrystallized from toluene-chloroform and the solid was discarded. The recrystallization mother liquors were evaporated in vacuo and the oily residue was triturated under 1N hydrochloric acid and then dissolved in dichloromethane. This latter solution was dried (MgSO4) and evaporated in vacuo to give 5.2 g of the title compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808597
Source datasetuspto-grants-1989_02
ORD IDord-283b7b7813694d2daa51ed6208304d04
Source noteuspto-grants-1989_02