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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205973Generated: October 31, 2026

Hexane → HCID 53239248, compound

https://huagongshe.com/reaction/2205973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantN-bromobutanimideHCID 67184—
Reactant1-{[2-(Trimethylsilyl)ethoxy]methyl}-1H-pyrrole-2-carbaldehydeHCID 13211462—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53239248HCID 5323924885.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrole-2-carbaldehyde (4.51 g) in THF (79 mL) was added NBS (4.27 g) at −20° C., and the mixture was stirred at 0° C. for 6 hr. To the reaction mixture was added hexane (240 mL), the precipitate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (5.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371320B2
Source datasetuspto-grants-2016_06
ORD IDord-44539a3692b74b8bae538d5c617848c8
Source noteuspto-grants-2016_06