HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 18981768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3,5-Dichlorobenzaldehyde | HCID 35746 | — |
| Reactant | 3-Aminopropyl-cyclohexylmethylphosphinic acid | HCID 130022 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18981768 | HCID 18981768 | — |
Reaction Steps
2.0 g of sodium cyanoborohydride are added in portions to a solution of 6.27 g of 3-aminopropyl-(cyclohexylmethyl)-phosphinic acid and 5.0 g of 3,5-dichlorobenzaldehyde and 1.91 g of glacial acetic acid in 50 ml of anhydrous methanol and the mixture is stirred at room temperature for 4 days. The solvent is removed, the white residue is taken up in 2.0M hydrochloric acid and filtered. The filtrate is concentrated to dryness by evaporation and the white solid that remains behind is suspended in ethyl acetate, filtered off and crystallised from propanol, yielding 3-[(3,5-dichlorobenzyl)-amino]-propyl-(cyclohexylmethyl)-phosphinic acid, m.p. 231°-233°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05376684 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-b0c36e90d8fa4cfcb17b153321dd772a |
| Source note | uspto-grants-1994_12 |