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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623733Generated: October 30, 2026

Sodium hydride → HCID 14462625, compound

https://huagongshe.com/reaction/623733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantHCID 86711822HCID 86711822—
SolventDimethylformamideHCID 6228—
ProductHCID 14462625HCID 14462625118.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl 1-(3-chlorobenzyl)-3-(4-chlorophenyl)-4-methyl-1H-pyrrole-2-carboxylate (1 g, 3.79 mmol) in dry DMF (5 mL) was added dropwise to a cooled suspension of 60% NaH in mineral oil (0.167 g, 4.17 mmol) in dry DMF (5 mL). The mixture was stirred at 0° C. for 20 min, then 3-chlorobenzyl bromide (0.524 mL, 3.98 mmol) was added dropwise over 5 min. The mixture was stirred for 10 min at 0° C., then the cooling was removed and the stirring was continued for 2.5 h at room temperature. The reaction was quenched by the addition of saturated aqueous NH4Cl/ice (1:1, 50 mL) and the product was extracted with EtOAc (50 mL). The combined organic layers were dried on Na2SO4 and evaporated and the residual crude product purified using gravity column chromatography (silica, heptane/EtOAc 9:1) to give the desired product (1.18 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302988B2
Source datasetuspto-grants-2016_04
ORD IDord-0293a7df2e5242448a26736431845f41
Source noteuspto-grants-2016_04