Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354489Generated: October 30, 2026

Oxalyl chloride → HCID 21054123, compound

https://huagongshe.com/reaction/2354489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiethyl decylphosphonateHCID 2773697—
SolventDiethyl EtherHCID 3283—
ProductHCID 21054123HCID 2105412373%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a 500 mL round bottomed flask containing n-decylphosphonic acid diethyl ester, 22 g (79.0 mmol) was added to 100 mL of diethylether. This solution was stirred and cooled to −20° C. using an ice/salt water bath. Oxalyl Chloride (20.06 g, 158 mmol) was added in small portions over 45 minutes while maintaining the temperature at −20° C. The reaction mixture was then allowed to warm to room temperature and stirred for 24 hours. The solvent was removed by rotary evaporation to give a viscous liquid. The liquid was purified by vacuum distillation (boiling point: 126° C. at 0.4 mmHg) to give 15.5 g (73% yield) of the desired product. 1H NMR (400 MHz CDCl3): δ 4.2 (m, 2H), 2.0 (m, 2H), 1.6 (m, 2H), 1.2 (m, 17H), 0.75 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754200B2
Source datasetuspto-grants-2010_07
ORD IDord-78f8cefa24474132824a1320633dcd3e
Source noteuspto-grants-2010_07