HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-Iodo-4,5-dimethoxybenzoic acid | HCID 2758422 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate | HCID 67087805 | 95% |
Reaction Steps
To a stirred solution of 2-iodo-4,5-dimethoxybenzoic acid (24.6 g, 80 mmol), ethyl 2-aminoacetate hydrochloride (11 g, 88 mmol), EDCl (17 g, 88 mmol) and HOBt (14 g, 88 mmol) in dry DCM (500 mL) was added Et3N (55 mL, 400 mmol) dropwise at rt. The resulting mixture was stirred at room temperature overnight then the reaction was quenched with water, and thoroughly extracted with DCM. The combined organic phases were washed with brine and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using petroleum ether/ethyl acetate 3:1 (v:v) as eluent to give ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate (29 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062076B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-69c2e5e7112d483f807a47575309e914 |
| Source note | uspto-grants-2015_06 |