Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 59314255 | HCID 59314255 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 59314362 | HCID 59314362 | 88% |
Reaction Steps
A 100 mL flask containing 5-bromo-2-cyclobutoxy-3-methyl-benzoic acid methyl ester (2.07 g, 7.25 mmol) as prepared above is charged with 1,4-dioxane (12 mL) and MeOH (12 mL). A stirring bar is added and stirring is initiated. After dissolution, water (6 mL) is added followed by the LiOH (768 mg, 18.3 μmol). After 18 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%, ˜11 mL). The contents of the flask are poured into a separatory funnel which contains EtOAc (50 mL). The layers are separated. The aqueous layer is extracted with EtOAc (40 mL). The combined organic phases are washed with water (40 mL) and brine (40 mL), dried over MgSO4, filtered and concentrated by pumping to constant weight to give a white solid (1.82 g, 88%).
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-548bf8d4e9964f28b8300862a8ab6a5c |
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| Source note | uspto-grants-2013_10 |
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