Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl dichlorophosphate | HCID 69611 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl o-phenylene phosphate | HCID 12617050 | 129.5% |
Reaction Steps
To 1.418 g of pyrocatechol were added 1.917 g of methyl dichlorophosphate and 11 ml of acetonitrile. The mixture was cooled to -25° C. and 2.605 g of triethylamine was added dropwise at -25° C. to -20° C. with stirring. The dropping funnel was washed with 1 ml of acetonitrile and the washings were added to the mixture. After stirring at the same temperature for 10 minutes, the reaction mixture was allowed to return to 10° C. and then filtered. The filtration residue was washed with a 5-ml and 3-ml portion of acetonitrile. The filtrate and washings were concentrated under reduced pressure on a water bath at 15° C. to 20° C. to give 3.102 g of methyl o-phenylene phosphate as a slightly turbid oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801703 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-61fd07b5e0394236a777823d6f4faa4f |
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| Source note | uspto-grants-1989_01 |
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