HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → N-formyl-3,4-dimethoxy-6-iodo-L-phenylalanine ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | N-formyl-3,4-dimethoxy-L-phenylalanine ethyl ester | HCID 10945877 | — |
| Catalyst | Silver trifluoroacetate | HCID 76299 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-formyl-3,4-dimethoxy-6-iodo-L-phenylalanine ethyl ester | HCID 11122367 | 75.3% |
Reaction Steps
Iodine (2.1 g, 8.3 mmol) was added to a solution of dimethoxy derivative 2 (2.1 g, 7.5 mmol) and silver trifluoroacetate (2.0 g, 9.1 mmol) in methylene chloride (110 mL) and the reaction mixture was stirred at room temperature for 48 h. The yellow precipitate that formed was filtered and washed with methylene chloride. The combined filtrates were washed with 1M Na2S2O5 (2×75 mL), water (2×75 mL), dried and concentrated under reduced pressure to give a solid residue. Recrystallization of this residue from ethyl acetate and petroleum ether gave a white solid 3 (2.3 g, 75%); m.p. 151°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05393908 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-41f614f33f9049788b0b5e1e6c9b4ab4 |
| Source note | uspto-grants-1995_02 |