HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86744246, compound → HCID 14884231, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86744246 | HCID 86744246 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 14884231 | HCID 14884231 | — |
Reaction Steps
A solution of 38 g of the ester in 400 ml ethanol and 200 ml of 1.5N aqueous sodium hydroxide is stirred at room temperature for 16 hours. The ethanol is evaporated at 50° and reduced pressure and the basic solution is washed with ethyl acetate, made acidic with ice cold 5N aqueous hydrochloric acid and extracted into ethyl acetate; the extract is washed with brine, dried over MgSO4, treated with charcoal and filtered. The solvent is evaporated at 50° and reduced pressure and the residue is crystallized from ether to yield (E)-3-(1-cycloheptyl-1H-pyrrol-3-yl)-2-propenoic acid, m.p. 138°-140°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960787 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-d9c2004f1957423cb9efddffafbea64f |
| Source note | uspto-grants-1990_10 |