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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460239Generated: October 30, 2026

Iodine → HCID 19983093, compound

https://huagongshe.com/reaction/1460239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanesulfonic AcidHCID 6395—
ReactantFumaric AcidHCID 444972—
Reactant4-(Bis(4-fluorophenyl)methylene)piperidineHCID 2724436—
ReactantPhosphorusHCID 5462309—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 19983093HCID 1998309332%

Reaction Steps

A mixture of 30.6 g (0.99 mole) of phosphorous and 15.1 g (0.059 mole) of iodine in 90 ml of glacial acetic acid was stirred for 20 min at room temperature. A mixture of 6 ml of water, 70 ml of methanesulfonic acid, 56.19 g (0.197 mole) of 4-[bis(4-fluorophenyl)methylene]piperidine and 110 ml of glacial acetic acid was added, and the mixture was heated at reflux for 7 hr. The solvent was removed in vacuo, and the resulting viscous liquid was poured over ice. The icy mixture was made basic with 50% sodium hydroxide, and the basic suspension was extracted with methylene chloride. The methylene chloride solution was extracted with an aqueous solution of sodium thiosulfate and was dried over anhydrous sodium sulfate, and the solution was filtered through Celite®. The solvent was removed in vacuo to give a gum. The gum was dissolved in 400 ml of hot methanol, and 4.25 g of an unknown tan solid was collected from the warm solution. Fumaric acid (22 g, 0.19 mole) was added to the methanolic solution followed by the addition of ether. A white precipitate was collected to give 22.55 g (32%) of crystalline solid, mp 208°-209° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05070087
Source datasetuspto-grants-1991_12
ORD IDord-c7146135a93c45878e338ad5b94803a9
Source noteuspto-grants-1991_12