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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-(2-Trifluoromethyl-benzoylamino)-indan-2-carboxylic acid ethyl ester | HCID 59314376 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 2-(2-Trifluoromethyl-benzoylamino)-indan-2-carboxylic acid | HCID 59314332 | 97,336.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569535B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-713c78af71074b558fb8d5a53f3bc748 |
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| Source note | uspto-grants-2013_10 |
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