HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → N-(2,2-dimethoxy-ethyl)-5-nitro-isophthalamic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-(chlorocarbonyl)-5-nitrobenzoate | HCID 74774 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2,2-dimethoxy-ethyl)-5-nitro-isophthalamic acid methyl ester | HCID 67439609 | — |
Reaction Steps
Under ice cooling a solution of 22.1 g (90.7 mmol) of 3-chlorocarbonyl-5-nitro-benzoic acid methyl ester (U.S. Pat. No. 4,120,891) in 200 ml of DCM is added dropwise to a stirred suspension of 11.2 g (181 mmol) of K2CO3 and 11.7 ml (109 mmol) of aminoacetaldehyde dimethylacetal in 200 ml of DCM. The mixture is stirred at ambient temperature for 2 days, diluted with ethyl acetate and extensively washed with water. The organic phase is dried over sodium sulfate and evaporated to yield the product in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039455B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-5168e8333bb54d3397d3ae3a4e195b8b |
| Source note | uspto-grants-2011_10 |