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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105723Generated: November 1, 2026

Formaldehyde → HCID 12832600, compound

https://huagongshe.com/reaction/1105723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantDiethylphosphiteHCID 3780918—
ReactantSodiumHCID 5360545—
SolventDiethyl EtherHCID 3283—
ProductHCID 12832600HCID 1283260015.9%

Reaction Steps

To a stirred solution of 5.8 grams (0.25 mole) of sodium metal in 150 ml of diethyl ether, under an argon atmosphere and at 15°-20°, was added dropwise 34.5 grams (0.25 mole) of diethyl phosphite. Complete addition required 60 minutes. Upon completion of the addition, the reaction mixture was kept at 15°-20° for 1 hour, then heated under reflux for 1 hour. The reaction mixture was cooled to 15° and 9.0 grams (0.30 mole) of paraformaldehyde was added in portions during a 10-15 minute period. Upon completion of the addition the reaction mixture was stirred at ambient temperature for 18 hours. After this period 52.4 grams (0.25 mole) of 2,6-dichlorobenzoyl chloride in 50 ml of diethyl ether was added dropwise during a 37-minute period. Upon completion of the addition the reaction mixture was stirred for 1.5 hours, then filtered. The filtrate was evaporated under reduced pressure to a residual oil. Impurities were removed from the residual oil by high vacuum distillation. The pot residue was subjected to column chromatography on 600 grams of silica gel using ethyl acetate as eluent. The appropriate fractions were combined and distilled under high vacuum to give 13.6 grams of diethyl (2,6-dichlorobenzoyloxy)methylphosphonate; bp 164°-167°/0.01 mm. The nmr and the ir spectra were consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309566
Source datasetuspto-grants-1982_01
ORD IDord-12e4d6bc805245afb1a3913b7a3c5ead
Source noteuspto-grants-1982_01