HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674437Generated: October 30, 2026
Hydrogen Peroxide → HCID 178455779, compound
https://huagongshe.com/reaction/1674437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178455776 | HCID 178455776 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178455779 | HCID 178455779 | 50.9% |
Reaction Steps
37 g of 2,3-difluoro-1-(trans-4-ethylcyclohexyl)methoxybenzene was dissolved in 222 mL of THF, and 59.9 mL of butyllithium (2.67 M hexane solution) was added dropwise thereto at an internal temperature of −40° C. or lower. Then, further stirring was continued for 30 min. To this solution, 18.1 g of trimethyl borate was added dropwise at an internal temperature of −40° C. or lower, and then the temperature was increased to 0° C. Then, 24.7 mL of 30% hydrogen peroxide solution was added dropwise for 5 min, and the stirring was continued for 3 hours. Water and toluene were added thereto, and the organic layer was fractioned while the aqueous layer was extracted with toluene. The organic layers were combined and washed with water, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography, to thereby obtain 20 g of 2,3-difluoro-4-(trans-4-ethylcyclohexyl)methoxyphenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003006B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8ff1c2e48b7e4e9b88097487ba678c1b |
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| Source note | uspto-grants-2011_08 |
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