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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515873Generated: October 30, 2026

Sodium hydride → HCID 117833828, compound

https://huagongshe.com/reaction/515873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzene, ((2-bromoethoxy)methyl)-HCID 73833—
ReactantEthyl 2-methyl-3-pyrrolecarboxylateHCID 136747—
SolventDimethylformamideHCID 6228—
ProductHCID 117833828HCID 117833828—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-methyl-1H-pyrrole-3-carboxylate (10 g, 65.3 mmol) is dissolved in 100 mL of dimethylformamide under argon cooled to 0° C., and then 2-bromoethoxymethylbenzene (28.1 g, 130.6 mmol) is added all at once. The reaction mixture is placed under stirring. There is then added thereto, at 0° C., in three portions, NaH (1.72 g, 71.83 mmol) over a period of 15 minutes. The reaction mixture is stirred for 15 minutes at 0° C., and then for 15 hours at ambient temperature. It is then poured into an ice bath and then extracted 3 times with ethyl acetate. The organic phase is washed 3 times with saturated aqueous lithium chloride solution, dried over MgSO4, filtered and then evaporated to dryness. The residue thereby obtained is purified by chromatography over silica gel using petroleum ether and ethyl acetate as eluants. The expected compound is obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-bec706430c454942bc6daea26e906a29
Source noteuspto-grants-2015_08