HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → N-[2-(4-acetamidobutyryl)-5-chlorohydrocinnamoyl]glycine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Glycine, N-(3-(2-(4-(acetylamino)-1-oxobutyl)-5-chlorophenyl)-1-oxopropyl)-, ethyl ester | HCID 3078712 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[2-(4-acetamidobutyryl)-5-chlorohydrocinnamoyl]glycine | HCID 19838947 | — |
Reaction Steps
15 ml of 2N sodium hydroxide solution are added to a solution of 1.50 g (0.004 mol) of ethyl N-[2-(4-acetamidobutyryl)-5-chlorohydrocinnamoyl]glycinate in 15 ml of tetrahydrofuran and the mixture is stirred at room temperature for 1 hour. After acidification with 17 ml of 2N hydrochloric acid, the mixture is extracted with ethyl acetate/water, dried with magnesium sulfate and the solvent is distilled in a vacuum. Recrystallization from ethyl acetate/ether yields N-[2-(4-acetamidobutyryl)-5-chlorohydrocinnamoyl]glycine as white crystals with melting point 88°-89°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04883815 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-2c5993a40e184717ae3127ac009c8f5e |
| Source note | uspto-grants-1989_11 |