Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 69831028 | HCID 69831028 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69830469 | HCID 69830469 | — |
Reaction Steps
To a solution of 2-diazo-1-[3-(2,2-dimethyl-[1,3]-dioxolan-4-ylmethoxy)-2-methylphenyl]ethanone (0.5 g, 1.73 mmol) in 20 mL of methanol at room temperature was added dropwise a solution of silver benzoate (52 mg, 13%) in 2.6 mL of triethylamine. The solution turned greenish and then brown, black precipitate formed. After stirring for 1.5 h, it was filtered through celite and the filtrate was concentrated. The residue was then purified on a silica gel column with 20% ethyl acetate in hexane to afford 0.43 g of [3-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-2-methylphenyl] acetic acid methyl ester. The above ester was then hydrolyzed by stirring with lithium hydroxide (0.25 g) in 5 mL of methanol at room temperature to give 0.4 g of [3-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-2-methylphenyl] acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479490B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-3b80364d463d42b19e258503cb457717 |
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| Source note | uspto-grants-2002_11 |
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