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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079411Generated: November 1, 2026

Water → HCID 23366935, compound

https://huagongshe.com/reaction/1079411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
ReactantHCID 23366945HCID 23366945—
SolventAcetoneHCID 180—
ProductHCID 23366935HCID 2336693521.9%

Reaction Steps

To a solution of 1-tert-butyloxycarbonyl-4-(4-tert-butyloxycarbonylaminophenyloxy)piperidine (0.9 g) in acetone (20 ml) were added solid potassium hydroxide (0.13 g) and 3-methyl-2-butenyl bromide (0.34 g) and the mixture was heated under reflux overnight. Water was added to the reaction mixture and the mixture was extracted with methylene chloride (50 ml×3). The combined organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off. The resulting residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=4/1 (v/v)) to obtain 1-tert-butyloxycarbonyl-4-[4[N-tert-butyloxycarbonyl-N-(3-methyl-2-butenyl)amino]-phenyloxy]piperidine (0.23 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580883
Source datasetuspto-grants-1996_12
ORD IDord-9ec80b5bb2004e9095271390e1b15775
Source noteuspto-grants-1996_12