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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047919Generated: November 2, 2026

Methanol → 2-(2-Trifluoromethyl-benzoylamino)-indan-2-carboxylic acid

https://huagongshe.com/reaction/1047919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant1,4-DioxaneHCID 31275—
Reactant2-(2-Trifluoromethyl-benzoylamino)-indan-2-carboxylic acid ethyl esterHCID 59314376—
SolventDichloromethane methanolHCID 21226129—
Product2-(2-Trifluoromethyl-benzoylamino)-indan-2-carboxylic acidHCID 5931433297,336.5%

Reaction Steps

A 100 mL flask containing 2-(2-trifluoromethyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (324, 0.57 g, 1.5 μmol) is charged with 1,4-dioxane (9 mL) and MeOH (9 mL). A stirring bar is added and stirring is initiated. After dissolution, water (4.5 mL) is added followed by the LiOH monohydrate (160 mg, 3.81 mmol). After 110 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%, ˜9 mL). The contents of the flask are poured into a separatory funnel which contains EtOAc (40 mL). The layers are separated. The aqueous layer is extracted with EtOAc (20 mL). The combined organic phases are washed with water (20 mL) and brine (20 mL), and then dried over MgSO4, filtered and concentrated by pumping to constant weight yields off white solid (0.51 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-713c78af71074b558fb8d5a53f3bc748
Source noteuspto-grants-2013_10