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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065612Generated: October 31, 2026

Pyridine → HCID 11335795, compound

https://huagongshe.com/reaction/1065612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactantdiethoxyphosphoryl-phenyl-methanolHCID 238674—
SolventDichloromethaneHCID 6344—
ProductHCID 11335795HCID 1133579572.9%

Reaction Steps

90 g of bromine, dissolved in 250 ml of methylene chloride, were added dropwise to a solution of 131 g (0.5 mole) of triphenylphosphine in 500 ml of methylene chloride at 30° to 35° C., moisture being excluded. The mixture was subsequently stirred at room temperature for 1 hour, a solution of 122 g (0.5 mole) of α-hydroxybenzyl-phosphonic acid diethyl ester in 250 ml of methylene chloride was then added dropwise at -20° C. in the course of 1 hour, the mixture was subsequently stirred at -20° C. for 1 hour and 40 g of pyridine, dissolved in 250 ml of methylene chloride, were then added dropwise at -20° C. in the course of one hour. The mixture was subsequently stirred for 20 hours, whereupon the temperature rose slowly to +20° C. The reaction mixture was transferred to a pear-shaped flask and the solvent was distilled off under a waterpump vacuum. The residue was extracted by stirring with one liter of ether and the undissolved triphenylphosphine oxide was filtered off (120 g of triphenylphosphine oxide=86% of theory). The mother liquor was concentrated in vacuo and the residue distilled under a high vacuum. 112 g (72% of theory) of α-bromobenzylphosphonic acid diethyl ester were obtained as a light yellow oil with a boiling point of 110° C./0.01 mm Hg and a purity of 95.9% (gas chromatogram).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04330482
Source datasetuspto-grants-1982_05
ORD IDord-27ebc92d75904881bcbb14a612cfe065
Source noteuspto-grants-1982_05