HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-hydroxy-2-(4-methoxyphenyl)acetate → N-(2-chloro-3,4-dimethoxyphenylethyl)-4-methoxymandelamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-hydroxy-2-(4-methoxyphenyl)acetate | HCID 523496 | — |
| Reactant | 2-Chloro-3,4-dimethoxyphenethylamine | HCID 3017752 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-chloro-3,4-dimethoxyphenylethyl)-4-methoxymandelamide | HCID 13697589 | 69.4% |
Reaction Steps
16.86 g of (2-chloro-3,4-dimethoxyphenyl)ethylamine obtained in step 4 was reacted with 15.33 g of methyl 4-methoxymandelate obtained in step 5 at 130° to 140° C. in a nitrogen gas atmosphere for 1.5 hour. After cooling, the reaction mixture was dissolved in 30 ml of ethyl acetate and purified by silica gel chromatography. After development with ethyl acetate/n-hexane (1/1) and then with ethyl acetate, 20.6 g (69%) of N-(2-chloro-3,4-dimethoxyphenylethyl)-4-methoxymandelamide was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05292521 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-827adb5039cf44319fd43a564404c0cf |
| Source note | uspto-grants-1994_03 |