HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 4-methoxyphenyl ketone → HCID 67621352, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 86751513 | HCID 86751513 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67621352 | HCID 67621352 | 81.9% |
Reaction Steps
Using the procedure described in example 5, treatment of L-proline-L-isoleucine benzylamide (208 mg, 0.65 mmol), with sodium carbonate (104 mg, 0.98 mmol), and 2-bromo-4'- methoxyacetophenone (195 mg, 0.85 mmol, 1.3 eq) in MeOH (10 mL), provided 248 mg (81%) of L-isoleucine, N-[1-(2-(4-methoxyphenyl)-2-oxoethyl)-L-prolyl] benzylamide as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686424 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-0165b76f40f94ee78cd0c6a628ddfbe6 |
| Source note | uspto-grants-1997_11 |