Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Chlorophenol | HCID 7933 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl N-trifluoroacetyl-N-(dichlorophosphonomethyl)glycinate | HCID 23345669 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53930935 | HCID 53930935 | 67.2% |
Reaction Steps
A solution of ethyl N-trifluoroacetyl-N-(dichlorophosphonomethyl)glycinate (8.25 g, 0.025 mole) in 100 ml. of ether was cooled to 0° C. and treated with a solution of methanol (1.01 ml, 0.025 mole) and triethylamine (3.49 ml, 0.025 mole) in 100 ml. of ether. After two hours, the mixture was filtered and the filtrate was cooled to 0° C. and treated with a solution of m-chlorophenol (3.21 g, 0.025 mole) and triethylamine (3.49 ml, 0.025 mole) in 100 ml. of ether. The resulting solution was stirred overnight at 25° C., filtered and the filtrate concentrated in vacuo. The residue was extracted into petroleum ether and the resulting solution was concentrated in vacuo to yield ethyl N-trifluoroacetyl-N-(methoxy(m-chlorophenoxy)phosphonomethyl)glycinate as a yellow oil (7.55 g), ND =1.4803.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04180394 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-6d21b37aeab14985a6ad1ff0287eff0d |
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| Source note | uspto-grants-1979_12 |
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