HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-[N-(2-Benzyloxy-5-bromobenzyl)aminomethyl]Benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate | HCID 22675503 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[N-(2-Benzyloxy-5-bromobenzyl)aminomethyl]Benzoic Acid | HCID 4720517 | 60.9% |
Reaction Steps
To a mixture of ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)-aminomethyl]benzoate (1.4 g) in methanol (25 ml) was added 2N sodium hydroxide solution (7.7 ml). The mixture was heated at reflux for 30 minutes, left to stand for 2 hours at ambient temperature, the solvent evaporated and the residue mixed with water (20 ml). The mixture was acidified with acetic acid, the precipitate filtered off and crystallised form ethyl acetate to give the title compound (800 mg) mpt 209° C. The starting material was prepared as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057345 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-ec3d0ba5fe944f74800dc8c14970af68 |
| Source note | uspto-grants-2000_05 |