Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | M-Xylene | HCID 7929 | — |
| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Product | Ethyl m-tolylacetate | HCID 96574 | 90% |
Reaction Steps
m-Xylene (1.59 g), ethanol (46 mg), di-tert-butyl peroxide (73 mg, 1 equivalent), and Pd(Xantphos)Cl2 (3.8 mg, 1 mol %) were added into a reaction kettle, into which 10 atm carbon monoxide was introduced. The reaction was heated to 120° C., and stirred at this constant temperature for 16 h. After the reaction was completed, carbon monoxide was discharged, and 80 mg ethyl m-methylphenylacetate was obtained by column chromatography, in a yield of 90%. 1HNMR (400 MHz, CDCl3) δ 1.23 (t, J=7.2 Hz, 3H), 2.33 (s, 3H), 3.57 (s, 2H), 4.12 (q, J=7.2 Hz, 2H), 7.06-7.09 (m, 3H), 7.19-7.24 (m, 3H); 13CNMR (100 MHz, CDCl3) δ14.2, 21.4, 41.4, 60.8, 126.3, 127.8, 128.5, 130.0, 134.1, 138.2, 171.8; HRMS (ESI) calcd. for C11H14NaO2 [M+Na]: 201.0886. found: 201.0887. The ethyl m-methylphenylacetate obtained was dissolved in 1,4-dioxane. 6 N sodium hydroxide solution was added, and the reaction was heated to 60° C. After 2 h of reaction, the pH value was adjusted to 1 by adding 2 N hydrochloric acid. After removing the organic solvent under reduced pressure, 63 mg product m-methylphenylacetic acid was obtained by extraction with ethyl acetate, and the yield of hydrolysis was 93%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921591B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-26e594ad622b42fbb44e7b9f38c5fa83 |
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| Source note | uspto-grants-2014_12 |
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