HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyraldehyde → n-benzyl-2-methylpropan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Phosphorous acid | HCID 107909 | — |
| Solvent | Water | HCID 962 | — |
| Product | n-benzyl-2-methylpropan-1-amine | HCID 211729 | — |
Reaction Steps
To the imine from isobutyraldehyde and benzylamine (51.4 g; 0.3 mole) was added phosphorous acid (24.6 g; 0.3 mole). While stirring the mixture was slowly warmed to 65°-70° when a vigorous exothermic reaction was initiated. The reaction temperature reached 130°-145°. Upon cooling the reaction mixture became a glass. This glass was dissolved in water and basified. Extraction with benzene yielded benzylisobutylamine. The aqueous portion was acidified and after removal of sodium chloride yielded a phosphonic acid (20 g). Recrystallization gave a white solid (12 g) mp 186°-190° the N-benzyl α-aminophosphonic acid. ##STR35##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04235809 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-c4b49112a199428c8473cdf55ff1b8ff |
| Source note | uspto-grants-1980_11 |