HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674447Generated: October 30, 2026
Hydrochloric Acid → HCID 178445647, compound
https://huagongshe.com/reaction/1674447
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Reactant | HCID 178445646 | HCID 178445646 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 178445647 | HCID 178445647 | — |
Reaction Steps
3 g of 1-((trans-4-(3-butenyl)cyclohexyl)methoxy)-2,3-difluorobenzene was dissolved in 30 mL of THF, and 11.7 mL of sec-butyllithium (1.01 M cyclohexane, a hexane solution) was added dropwise thereto at an internal temperature of −40 to −60° C. Then, the solution was stirred for 30 min. To this solution, 1.3 g of trimethyl borate was added, and the solution was heated to room temperature. Then, 1.8 mL of 30% hydrogen peroxide solution was added thereto, and the solution was stirred at 40° C. for 1 hours. To the solution, 5% hydrochloric acid was added, and the solution was stirred for 1 hour. Toluene was added thereto, and the organic layer was fractioned, washed with saturated saline, and then dried over anhydrous magnesium sulfate, to thereby obtain 4-((trans-4-(3-butenyl)cyclohexyl)methoxy)-2,3-difluorophenol.
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-da31357484084469a67d517d1f88a9c7 |
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| Source note | uspto-grants-2011_08 |
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