HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113813Generated: October 28, 2026
Water → Methyl 3-hydroxy-5-isopropoxybenzoate
https://huagongshe.com/reaction/2113813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3,5-Dihydroxybenzoate | HCID 75076 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-hydroxy-5-isopropoxybenzoate | HCID 23072925 | 30,042.801% |
Reaction Steps
After adding 41.0 g (0.30 mmol) of potassium carbonate and 23.8 g (0.19 mmol) of 2-bromopropane to a solution of 25.0 g (0.15 mol) of 3,5-dihydroxybenzoic acid methyl ester in N,N-dimethylformamide (250 ml), the reaction mixture was stirred at 80° C. for 4 hours. Water was added to the reaction mixture, extraction was performed with acetic acid ethyl ester, and then the organic layer was washed with brine, dried and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=5:1) to obtain 12.0 g of 5-hydroxy-3-isopropoxybenzoic acid methyl ester (yield: 38%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432287B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-75240f6ae57d485f8feb8edd7a29b7c2 |
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| Source note | uspto-grants-2008_10 |
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