HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047820Generated: October 30, 2026
Methanol → 2-[(2-Methylsulfonylbenzen-1-carbonyl)-amino]-indan-2-carboxylic acid
https://huagongshe.com/reaction/1047820
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-[(2-Methylsulfonylbenzen-1-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester | HCID 59314139 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol methylene chloride | HCID 21966342 | — |
| Product | 2-[(2-Methylsulfonylbenzen-1-carbonyl)-amino]-indan-2-carboxylic acid | HCID 59314323 | 100.8% |
Reaction Steps
A 50 mL flask containing 2-[(2-methylsulfonylbenzene-1-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (186, 0.50 g, 1.27 mmol) is charged with 1,4-dioxane (5 mL) and MeOH (5 mL). A stirring bar is added and stirring is initiated. After dissolution, water (2.5 mL) is added followed by the LiOH (133 mg, 3.17 mmol). After 69 h, tlc analysis (silica, 5% i-PrOH/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%, ˜12 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. Pumping to constant weight gives 0.46 g of 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-e718040cbd8f4cf1a516c2067933c19d |
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| Source note | uspto-grants-2013_10 |
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