HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → N-methyl-N-(2-ethoxycarbonylbenzyl)-3-ethoxycarbonylmethylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 2-(bromomethyl)benzoate | HCID 11032082 | — |
| Reactant | Ethyl 2-[3-(methylamino)phenyl]acetate | HCID 23333594 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-methyl-N-(2-ethoxycarbonylbenzyl)-3-ethoxycarbonylmethylaniline | HCID 23333589 | 68.3% |
Reaction Steps
The starting material employed above had been synthesized in the same manner as described in Example 1. That is, N-methyl-3-ethoxycarbonylmethylaniline (20.7 g), sodium hydrogencarbonate (19 g), water (30 ml) and ethyl 2-bromomethylbenzoate (27.5 g) were used to produce N-methyl-N-(2-ethoxycarbonylbenzyl)-3-ethoxycarbonylmethylaniline (26 g) as a light yellow oil. Then, N-methyl-N-(2-ethoxycarbonylbenzyl)-3-ethoxycarbonylmethylaniline (26 g) so produced, sodium hydroxide (40 g), water (450 ml) and ethanol (150 ml) were used to prepare N-methyl-N-(2-carboxybenzyl)-3-carboxymethylaniline (14.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04230703 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-b81e8a66721f4dd297a595f6a93d028c |
| Source note | uspto-grants-1980_10 |