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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111716Generated: November 3, 2026

Methyl iodide → 4-Bromo-2-(methoxymethyl)thiophene

https://huagongshe.com/reaction/2111716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(4-Bromo-2-thienyl)methanolHCID 2795484—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-2-(methoxymethyl)thiopheneHCID 15018312—

Reaction Steps

Add sodium hydride (737 mg, 29.23 mmol, 1.10 equivalents, 95%) to a solution containing methyl iodide (1.65 mL, 26.57 mmol, 1.00 equivalents) and (4-bromo-thiophen-2-yl)-methanol (5.13 g, 26.57 mmol, 1.00 equivalents) in tetrahydrofuran (dry, 25 mL). Stir the resulting mixture at room temperature overnight and evaporate. Partition the residue between water (100 mL) and dichloromethane (100 mL). Extract the aqueous layer with dichloromethane (100 mL), combine the organic layers, dry over magnesium sulfate, filter and evaporate to yield the desired product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521445B2
Source datasetuspto-grants-2009_04
ORD IDord-ddaebcb2f40b4be9aff3f5377e702ebf
Source noteuspto-grants-2009_04