HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 67869983, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | L-Phenylalanine, methyl ester | HCID 736234 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Product | HCID 67869983 | HCID 67869983 | — |
Reaction Steps
The synthesis of the benzylphenylalanine methyl ester is described in Scheme II-29. The imine is formed by treating phenylalanine methyl ester with benzaldehyde followed by deprotonation with lithium hexamethyldisilazide to generate the anion and alkylation with benzylbromide to give 1-benzylphenylalanine methyl ester 115. ##STR38##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05183810 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-6ebb698691ae4409b17a4ccc3138523f |
| Source note | uspto-grants-1993_02 |