HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Methyl 2-(4-ethoxy-4-oxobutanamido)-5-iodobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Butanoic acid, 4-chloro-4-oxo-, ethyl ester | HCID 84648 | — |
| Reactant | Methyl 2-amino-5-iodobenzoate | HCID 847811 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-(4-ethoxy-4-oxobutanamido)-5-iodobenzoate | HCID 66935113 | — |
Reaction Steps
To methyl 2-amino-5-iodobenzoate (i-a) (15 g, 54 mmol) was added 200 mL of CH2Cl2, followed by DIEA (9.4 mL, 54 mmol) and a catalytic amount of DMAP. Ethyl 4-chloro-4-oxobutanoate (Rc═Rd═H) (8.5 mL, 60 mmol) was added, and the reaction mixture was allowed to stir at room temperature overnight. The reaction mixture was then poured into 250 mL H2O, and the organic layer was washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to afford ii-a (22 g, 99%) as a pale yellow solid: MS m/z=406 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935694B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-a163bfd9748840959022c2bb5458f181 |
| Source note | uspto-grants-2011_05 |