Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59314199 | HCID 59314199 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol methylene chloride | HCID 21966342 | — |
| Product | HCID 59314250 | HCID 59314250 | 89% |
Reaction Steps
A 50 mL flask containing the 2-[(Benzo[b]thiophene-2-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (0.37 g, 1.01 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 (3.0 mL) is added followed by the LiOH (106 mg, 2.53 mmol). After 18 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%, ˜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. Pumping to constant weight gives 290 mg (89%) of dry white powder.
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-334b9c3b6c9844e3a9cdd211b2b708aa |
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| Source note | uspto-grants-2013_10 |
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