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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090653Generated: October 31, 2026

Water → tert-Butyl ((5-bromo-1H-pyrrol-3-yl)methyl)(methyl)carbamate

https://huagongshe.com/reaction/2090653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-butyl{[5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamateHCID 66924909—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Producttert-Butyl ((5-bromo-1H-pyrrol-3-yl)methyl)(methyl)carbamateHCID 5752214761%

Reaction Steps

tert-Butyl {[5-bromo-1-(phenylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate (1.0 g) was dissolved in a mixed solvent of tetrahydrofuran (15 mL) and methanol (5 mL), and 8 mol/L aqueous sodium hydroxide solution (1.5 mL) was added dropwise at not more than 10° C. After stirring at the same temperature for 4 hr, water was added to the residue and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→4:1) to give the title compound as a pale-yellow oil (yield 410 mg, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436187B2
Source datasetuspto-grants-2013_05
ORD IDord-f9102a90f2ec4f1fbfca4e803b07482d
Source noteuspto-grants-2013_05