HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl 3-(4-chlorobenzoylamino)-3-(3-thienylcarbonyl)propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(4-chlorobenzoyl)-N-[(3-thienylcarbonyl)methyl]amine | HCID 13105428 | — |
| Product | Ethyl 3-(4-chlorobenzoylamino)-3-(3-thienylcarbonyl)propionate | HCID 13105432 | 71.9% |
Reaction Steps
15.0 g of N-(4-chlorobenzoyl)-N-[(3-thienylcarbonyl)methyl]amine, 3.1 g of 50% sodium hydride and 10 g of ethyl bromoacetate are treated in the same manner as described in Preparation 1-(4). 14.1 g of ethyl 3-(4-chlorobenzoylamino)-3-(3-thienylcarbonyl)propionate are thereby obtained. Yield: 71.4%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04460596 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-e1ce4e3b7cbc41ec9a4621eb6ce60c37 |
| Source note | uspto-grants-1984_07 |