Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 99798 | HCID 99798 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12874246 | HCID 12874246 | 99% |
Reaction Steps
9.2 g (0.0768 mol) of thionyl chloride were added to a mixture of 20.2 g (0.0725 mol) of 4-methoxy-α-hydroxy-benzyl-phosphonic acid diethyl ester, 65 g of methylene chloride and 5.8 g (0.0725 mol) of pyridine at 20°-40° C. in the course of about 1 hour, while cooling slightly with water. The reaction mixture was then heated under reflux for 3 hours and subsequently stirred for 12 hours, without further action of heat. The mixture was poured into about 100 g of ice-water and the organic phase was separated off and dried. After distilling off the solvent, the residue was concentrated under 6 mm Hg and at 45° C. 21 g (97.7% of theory) of 4-methoxy-α-chlorobenzyl-phosphonic acid diethyl ester were obtained as a yellow viscous oil with a purity of 98.6% (gas chromatogram) and with a refractive index of nD24 : 1.5118.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04327025 |
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| Source dataset | uspto-grants-1982_04 |
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| ORD ID | ord-166458f4ff60406880d6cb1ff4a923f7 |
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| Source note | uspto-grants-1982_04 |
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