HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7468Generated: October 26, 2026
Ethyl Acetate → 1,3-Benzenediol, 4-methyl-
https://huagongshe.com/reaction/7468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Benzene, 2,4-dimethoxy-1-methyl- | HCID 96403 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 1,3-Benzenediol, 4-methyl- | HCID 10333 | 94.1% |
Reaction Steps
The starting material 2,4-dihydroxytoluene was prepared by adding boron tribromide (3.1 ml, 3.2 mmol) to a solution of 2,4-dimethoxytoluene (1 g, 6.5 mmol) in pentane (10 ml) at −70° C. The reaction mixture was allowed to warm to ambient temperature and the mixture stirred for a further 2 hours. Ice water and ethyl acetate were then added and the aqueous layer basified to pH9.5 with 2M aqueous sodium hydroxide solution. After stirring for 10 minutes, the organic layer was separated and the aqueous layer extracted with ethyl acetate. The combined organic extract was washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by flash chromatography eluting with methylene chloride/ethyl acetate (9/1) to give 2,4-dihydroxytoluene (759 mg, 94%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087602B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-9e8621af0b5e4a71bd5b08d7280c5cb2 |
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| Source note | uspto-grants-2006_08 |
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