HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 22907290, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Reactant | HCID 178438097 | HCID 178438097 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22907290 | HCID 22907290 | 54.2% |
Reaction Steps
To a solution of ethyl 7-tert-butyl-2,3-dihydro-3,3-dimethylbenzofuran-5-carboximidic acid hydrochloride (400 mg, 1.29 mmol) in dioxane (10 mL) is added excess pyrrolidine (0.6 mL). A color change from red to yellow is observed during the addition, and a precipitate forms. The reaction is also monitored by TLC (10% MeOH/CHCl3). After 3 h, the yellow precipitate is collected by filtration and purified by preparative TLC (10% MeOH/CHCl3) to give the desired product as a white powder (210 mg, 54.2%), mp=255°-256° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05672620 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-9c7e101cd8e64f75b227e90ffad9419a |
| Source note | uspto-grants-1997_09 |