HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-Hydroxyethyl 4-(4-chlorophenyl)pyrrole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 2-(4-Chlorophenyl)-3-carbethoxymethylaminoacrylaldehyde | HCID 73165322 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxyethyl 4-(4-chlorophenyl)pyrrole-2-carboxylate | HCID 13064273 | — |
Reaction Steps
2-(4-Chlorophenyl)-3-carbethoxymethylaminoacrylaldehyde (73.6 g.) was refluxed in 300 ml. of ethylene glycol for 10 minutes. The reaction mixture was cooled, diluted with 1 liter of water, product extracted into chloroform, treated with activated carbon and evaporated to solids. Trituration with ether gave crude product (8 g.). An additional quantity of crude product (7.5 g.) crystallized from the aqueous phase which had been standing. Recrystallization of the combined crude solids from chloroform gave 2-hydroxyethyl 4-(4-chlorophenyl)pyrrole-2-carboxylate (5 g., m.p. 128°-130° C.). The ether and chloroform mother liquors were combined and evaporated to yield an additional 40 g. of crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282242 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-4a487cf9cbe5424bbd212e26e95144bd |
| Source note | uspto-grants-1981_08 |