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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067939Generated: October 29, 2026

Methyl iodide → HCID 68709761, compound

https://huagongshe.com/reaction/2067939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 68706611HCID 68706611—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68709761HCID 68709761—

Reaction Conditions

Temperature-75 °C

Reaction Steps

To a −78° C. solution of 4.06 g of 5-(4-Fluoro-phenyl)-4-iodo-1-methyl-1H-pyrazole-3-carboxylic acid ethyl ester in 80 mL of dry THF were added dropwise 8.13 ml of a 1.6 M solution of n-Butyllithium in THF maintaining the temperature below −70° C. The solution was stirred for 15 min at −75° C. and 1.4 ml of Methyl iodide was added. The reaction mixture was stirred for 30 min at −75° C. and allowed to warm up to room temperature. The mixture was worked up with Ethyl acetate and brine. The combined organic extracts were dried with magnesium sulfate, filtered and evaporated. The crude product (3.15 g) was purified by chromatography on silica gel (Heptane/Ethyl acetate 2:1). The desired product was obtained as a yellow oil (1.00 g, 35%), which solidified on standing. MS: m/e=263.1 ([M+1]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293916B2
Source datasetuspto-grants-2012_10
ORD IDord-e1c408a2051d41bbba4ad04228935926
Source noteuspto-grants-2012_10