Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2,6-Dichlorobenzoyl chloride | HCID 78392 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12832600 | HCID 12832600 | 15.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04309566 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-12e4d6bc805245afb1a3913b7a3c5ead |
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| Source note | uspto-grants-1982_01 |
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