Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Benzoic acid, 2,4-dihydroxy-3-methyl-, methyl ester | HCID 118521 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22169093 | HCID 22169093 | 37% |
Reaction Steps
To a solution of 2,4-dihydroxy-3-methylbenzoic acid methyl ester (9.9 g) in ethyl acetate (100 ml) was added tert-butyl hypochlorite (12.3 ml) under ice-cooling. After stirring for 2 hours, hexane (200 ml) was added, and the mixture was cooled with ice to allow precipitation of crystals. The crystals were collected by filtration, and dissolved in a mixed solvent of methanol (20 ml) and tetrahydrofuran (THF, 20 ml). A 1M lithium hydroxide solution (40 ml) was added to the solution, and the mixture was refluxed under heating for 18 hours. The reaction mixture was concentrated, and a 10% aqueous citric acid solution was added to the residue, which was followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to give the title compound (4.14 g, yield 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174887B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-92697b3fbd0041e6a4f4e17481d14e65 |
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| Source note | uspto-grants-2001_01 |
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