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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252531Generated: October 30, 2026

Tetrahydrofuran → HCID 66865449, compound

https://huagongshe.com/reaction/252531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 59426315HCID 59426315—
SolventWaterHCID 962—
ProductHCID 66865449HCID 6686544992%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-6303c2e190264e4eaf1c072ed18a9d5d
Source noteuspto-grants-2011_01