HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252531Generated: October 30, 2026
Tetrahydrofuran → HCID 66865449, compound
https://huagongshe.com/reaction/252531
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 59426315 | HCID 59426315 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66865449 | HCID 66865449 | 92% |
Reaction Steps
Methyl 4-(3-cyano-1-ethyl-5-methoxy-1H-indol-2-yl)-benzoate (350 mg, 1.05 mmol), prepared as described in Example 1Ga step B, is combined with NaOH (40 mg, 1 mmol), H2O (0.8 mL), and THF (3.4 mL) and is heated at 80° C. for 1 hour. The reaction mixture is diluted in H2O and is then ether-washed. The aqueous layer is acidified with aqueous HCl, and is extracted into EtOAc. The organic layer is dried and concentrated to yield 4-(3-cyano-1-ethyl-6-methoxy-1H-indol-2-yl)-benzoic acid (311 mg, 92%) as a pure white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07868037B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-6303c2e190264e4eaf1c072ed18a9d5d |
|---|
| Source note | uspto-grants-2011_01 |
|---|