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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674447Generated: October 30, 2026

Hydrochloric Acid → HCID 178445647, compound

https://huagongshe.com/reaction/1674447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantTrimethyl borateHCID 8470—
ReactantCID 53628100HCID 178418400—
ReactantHCID 178445646HCID 178445646—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventCyclohexaneHCID 8078—
ProductHCID 178445647HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003006B2
Source datasetuspto-grants-2011_08
ORD IDord-da31357484084469a67d517d1f88a9c7
Source noteuspto-grants-2011_08