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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-(3-Methyl-2-prop-2-ynyloxy-benzoylamino)-indan-2-carboxylic acid ethyl ester | HCID 59314111 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 2-(3-Methyl-2-prop-2-ynyloxy-benzoylamino)-indan-2-carboxylic acid | HCID 59314351 | 108% |
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
| 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-7000122e95c446a9ae9682768d8e532e |
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| Source note | uspto-grants-2013_10 |
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