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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986919Generated: October 27, 2026

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

https://huagongshe.com/reaction/1986919

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 numberUS07550469B2
Source datasetuspto-grants-2009_06
ORD IDord-347d4bec6cf843c78a0d9b49a746d612
Source noteuspto-grants-2009_06