Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Aminopiperidine | HCID 16658 | — |
| Reactant | Ethyl N-trifluoroacetyl-N-(dichlorophosphonomethyl)glycinate | HCID 23345669 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54239202 | HCID 54239202 | — |
Reaction Steps
A solution of phenol (2.3 g, 0.025 mole) and triethylamine (3.49 ml, 0.025 mole) in 50 ml. of ether was added to a solution of ethyl N-trifluoroacetyl-N-(dichlorophosphonomethyl)glycinate (8.25 g, 0.025 mole) in 150 ml. of ether at 0° C. After two hours, the solution was filtered and the filtrate was added to a cooled (0° C.) solution of N-aminopiperidine (5.2 ml, 0.05 mole) in 100 ml. of ether. The resulting solution was stirred at 25° C. for 16 hours, then filtered. The filtrate was washed with 0.3% hydrochloric acid, dried over sodium sulfate and concentrated in vacuo to afford ethyl N-trifluoroacetyl-N-(phenoxy(N-piperidinoamino)phosphonomethyl)glycinate which could not be further purified by any means.
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-55f22857c9f74aac86c01663204a3edd |
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| Source note | uspto-grants-1979_12 |
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