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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047830Generated: November 1, 2026

Methanol → 2-(3-Methyl-2-prop-2-ynyloxy-benzoylamino)-indan-2-carboxylic acid

https://huagongshe.com/reaction/1047830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
Reactant1,4-DioxaneHCID 31275—
Reactant2-(3-Methyl-2-prop-2-ynyloxy-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 59314111—
SolventWaterHCID 962—
SolventDichloromethane methanolHCID 21226129—
Product2-(3-Methyl-2-prop-2-ynyloxy-benzoylamino)-indan-2-carboxylic acidHCID 59314351108%

Reaction Steps

A 50 mL flask containing the 2-(3-methyl-2-prop-2-ynyloxy-benzoylamino)-indan-2-carboxylic acid ethyl ester (0.20 g, 0.53 mmol) is charged with 1,4-dioxane (3 mL) and MeOH (3 mL). A stirring bar is added and stirring is initiated. After dissolution, water (1.5 mL) is added followed by the LiOH (56 mg, 1.35 mmol). After 108 h, tlc analysis (silica, 10% MeOH/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%, ˜10 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 to constant weight to give 0.2 g of off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-7000122e95c446a9ae9682768d8e532e
Source noteuspto-grants-2013_10