HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → alpha-(3,5-Di-tert-butyl-4-hydroxyphenyl)-N-(3-phenylpropyl)-aminomethylphosphonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Diethyl alpha-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-phenylpropyl)aminomethylphosphonate | HCID 86748728 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-(3,5-Di-tert-butyl-4-hydroxyphenyl)-N-(3-phenylpropyl)-aminomethylphosphonic acid | HCID 86748727 | — |
Reaction Steps
Diethyl α-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-phenylpropyl)aminomethylphosphonate (compound 22, 3.0 g, 6.1 mmol) was heated at reflux in 30 ml NHCl for 24 h. The compound was extracted with chloroform, 2.5 g were obtained. Yield =94%, mp=162°-169° C. IR (KBr) 3640 cm-1 : OH, 3400 (broad): NH, 2800 and 1600: PO-H, 1430: tert-Bu, 1200: P=O, 1000 and 940: P--OH Elemental analysis: C24H36NO4P. % Calc. C 66.49 H 8.37 N 3.23 P 7.14 % Found C 66.69 H 8.52 N 2.95 P 6.91 0.2 % H2O
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424303 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-9a5b0306fe3c416398af18b29d37cc24 |
| Source note | uspto-grants-1995_06 |