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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523108Generated: October 26, 2026

Methyl iodide → 4-bromo-5-(methoxymethyl)-1-methyl-1H-pyrazole

https://huagongshe.com/reaction/523108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(4-bromo-1-methyl-1H-pyrazol-5-yl)methanolHCID 57415773—
SolventTetrahydrofuranHCID 8028—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
SolventSodium chloride; waterHCID 57417360—
Product4-bromo-5-(methoxymethyl)-1-methyl-1H-pyrazoleHCID 8999560467.2%

Reaction Steps

NaH (60%, 58 mg) was added to a solution of (4-bromo-1-methyl-1H-pyrazol-5-yl)methanol (Preparation 149, 97 mg, 1.03 mmol) in THF/DMF (8/4 mL). After stirring for 15 minutes, iodomethane (439 mg, 3.09 mmol) in THF (1 mL) was added. The resulting solution was stirred at room temperature for 16 hours. The reaction mixture was diluted with brine and extracted with EtOAc. The combined organic layers were washed with water, dried over sodium sulphate and concentrated in vacuo to afford the title compound (142 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334286B2
Source datasetuspto-grants-2016_05
ORD IDord-07e36eea7b7d45ccb68517445ea40eec
Source noteuspto-grants-2016_05