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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554203Generated: October 26, 2026

Methanol → Tert-butyl methyl[(5-phenyl-1H-pyrrol-3-YL)methyl]carbamate

https://huagongshe.com/reaction/554203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantMethylamineHCID 6329—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Phenyl-1H-pyrrole-3-carboxaldehydeHCID 11052090—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl methyl[(5-phenyl-1H-pyrrol-3-YL)methyl]carbamateHCID 5752214664%

Reaction Steps

To a solution (92 mL) of 5-phenyl-1H-pyrrole-3-carbaldehyde (0.92 g) in methanol was added 40% methylamine solution (1.26 g) at room temperature and the mixture was stirred for 30 min. To the reaction mixture was added sodium borohydride (305 mg) at room temperature and the mixture was stirred for 10 min. Water (200 mL) was added and the mixture was further stirred for 1 hr. Saturated brine (50 mL) was added 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 dissolved in acetonitrile (48 mL), and di-tert-butyl bicarbonate (1.41 g) was added dropwise at room temperature. The mixture was stirred for 1.5 hr and partitioned with water and ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→4:1) to give the title compound as colorless crystals (yield 0.99 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-ac3ca403bcfe44e396a957ac40052656
Source noteuspto-grants-2011_11