HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → N-benzylidene-D-phenylalanine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | D-Phenylalanine | HCID 71567 | — |
| Reactant | D-phenylalanine hydrochloride | HCID 13000988 | — |
| Product | N-benzylidene-D-phenylalanine methyl ester | HCID 24807472 | — |
Reaction Steps
To a suspension of 1.0 eq D-phenylalanine HCl (1.6 g, 7.4 mmol) was added 1.0 eq triethylamine to dissolve the D-phenylalanine. To this solution was added 1 equiv. of MgSO4 followed by the addition of 1.0 eq benzaldehyde, the reaction was stirred overnight at room temperature under N2 atmosphere. The reaction mixture was sripped of solvent and pumped on the residue contained a good deal of triethylamine hydrochloride which was removed by dissolving the product in THF and filtering out the TEA.HCl. The crude benzylidene looked fine by NMR and was all taken on in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246944 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-7a7c4c7f1f2e40e19f403a27972819ca |
| Source note | uspto-grants-1993_09 |