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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047822Generated: October 26, 2026

Methanol → 2-[(2,3-Dihydrobenzofuran-2-carbonyl)-amino]-indan-2-carboxylic acid

https://huagongshe.com/reaction/1047822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,4-DioxaneHCID 31275—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant2-[(2,3-Dihydrobenzofuran-2-carbonyl)-amino]-indan-2-carboxylic acid ethyl esterHCID 59314198—
SolventWaterHCID 962—
SolventIsopropanol methylene chlorideHCID 21966342—
Product2-[(2,3-Dihydrobenzofuran-2-carbonyl)-amino]-indan-2-carboxylic acidHCID 5931439995.7%

Reaction Steps

A 50 mL flask containing the 2-[(2,3-dihydrobenzofuran-2-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (0.447 g, 1.39 mmol) is charged with 1,4-dioxane (5 mL) and MeOH (5 mL). A stirring bar is added and stirring is initiated. After dissolution, water (2.5 mL) is added followed by the LiOH hydrate (133 mg, 3.17 mmol). After 19 h, tlc analysis (silica, 5% i-PrOH/DCM) indicates that the starting material is completely consumed. The pH of the reaction mixture is carefully adjusted to pH 2 by slowly adding dilute aqueous HCl (3%, ˜12 mL). The contents of the flask are poured into a separatory funnel containing EtOAc (30 mL). The layers are separated. The aqueous layer is extracted with EtOAc (20 mL). The combined organic extracts are washed with water (20 mL) and brine (20 mL), dried over MgSO4, filtered and concentrated. Pumping to constant weight gives 0.43 g of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-60541ecc22ee43d5a46305113345b88e
Source noteuspto-grants-2013_10