HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Cyclopentylmethoxy-1H-indole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Cyclopentylmethoxy-1H-indole-2-carboxylic acid ethyl ester | HCID 66841351 | — |
| Product | 4-Cyclopentylmethoxy-1H-indole-2-carboxylic acid | HCID 66841120 | — |
Reaction Steps
The 4-cyclopentylmethoxy-1H-indole-2-carboxylic acid ethyl ester 87 obtained above is mixed with a 2M-solution of KOH in EtOH (33.8 ml, 67.6 mmol) and stirred for 24 hours. The solvent is then evaporated and the residue is partitioned between water and ether. The water layer is acidified with HCl and extracted twice with EtOAc. The combined organic layers are washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated to give a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858781B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-281620a0e99b4ce099dfec8cc795a844 |
| Source note | uspto-grants-2010_12 |