HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzylamine → HCID 67763772, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10333694 | HCID 10333694 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67763772 | HCID 67763772 | — |
Reaction Steps
A mixture of 2.76 g of (2R)-3-chloro-2-hydroxypropyl(benzyl)phosphinic acid ethyl ester, 3.54 g of p-chlorobenzylamine, 3.25 g of N-ethyl-N,N-diisopropylamine and 20 ml of ethanol is heated under reflux for 48 hours. Removal of the solvent and chromatography yield (2S)-3-(p-chlorobenzylamino)-2-hydroxypropyl(benzyl)phosphinic acid ethyl ester; 1H--NMR spectrum (in CDCl3): δ=7.4-7.17 (9H,m); 4.14-3.83 (3H,m); 3.71 (2H,ABq); 3.20 (2H,d); 2.6-2.5 (2H,m); 1.96-1.62 (2H,m); 1.25 (3H,t); 31P--NMR spectrum (in CDCl3); δ=53.9; 52.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05545631 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-6663a20069504c2e87351c3c112aa235 |
| Source note | uspto-grants-1996_08 |