HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 54145704, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(3,4-dichlorophenyl)ethanamine | HCID 3159242 | — |
| Reactant | 3-chloro-2(R)-hydroxy-propyl(cyclohexylmethyl)phosphinic acid ethyl ester | HCID 10379061 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54145704 | HCID 54145704 | — |
Reaction Steps
A mixture of 4.24 g of 3-chloro-2(R)-hydroxy-propyl-(cyclohexylmethyl)-phosphinic acid ethyl ester, 2.85 g of 1-(3,4-dichlorophenyl)ethylamine, 1.95 g of Hunig base and 15 ml of ethanol is heated at reflux for 4 days. After cooling to room temperature and removal of the solvent under reduced pressure, the reaction mixture is partitioned between dichloro-methane and water, dried over sodium sulfate and again concentrated to dryness by evaporation. Chromatography on silica gel yields 3-{N-[1-(3,4-dichlorophenyl)ethyl]amino}-2(S)-hydroxy-propyl(cyclohexylmethyl)phosphinic acid ethyl ester, [α]20D =-1.8°±0.9° (c=1.079 in chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05500418 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-69d66983987c429489cde726c2f75842 |
| Source note | uspto-grants-1996_03 |