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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047910Generated: October 26, 2026

Methanol → 2-[(2,2-Difluoro-benzo[1,3]dioxole-4-carbonyl)-amino]-indan-2-carboxylic acid

https://huagongshe.com/reaction/1047910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant1,4-DioxaneHCID 31275—
Reactant2-[(2,2-Difluoro-1,3-benzodioxole-4-carbonyl)-amino]-indan-2-carboxylic acid ethyl esterHCID 59314165—
SolventDichloromethane methanolHCID 21226129—
Product2-[(2,2-Difluoro-benzo[1,3]dioxole-4-carbonyl)-amino]-indan-2-carboxylic acidHCID 5931435994%

Reaction Steps

A 100 mL flask containing 2-[(2,2-difluoro-1,3-benzodioxole-4-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (0.38 g, 0.98 mmol) is charged with 1,4-dioxane (6 mL) and MeOH (6 mL). A stirring bar is added and stirring is initiated. After dissolution, water (3 mL) is added followed by the LiOH monohydrate (103 mg, 2.46 mmol). After 70 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%, ˜6 mL). The contents of the flask are poured into a separatory funnel which contains 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 by pumping to constant weight to give off white solid (0.33 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-5516e07943a64b788dabf210adde8d75
Source noteuspto-grants-2013_10