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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054452Generated: October 26, 2026

Methyl iodide → Benzyl 1-methylcyclopropane-1-sulfonate

https://huagongshe.com/reaction/1054452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantButyl cyclopropanesulfonateHCID 10464888—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 1-methylcyclopropane-1-sulfonateHCID 8961860793%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-BuLi (0.78 g, 12.25 mmol) was added drop-wise at −78° C. to a solution of Butylcyclopropane sulfonate (2.0 g, 11.2 mmol) in THF (20 mL) and continued stirring at the same temperature for 10 min. CH3I (3.98 g, 28.0 mmol) was added at −78° C., allowed the reaction to warm to 0° C. with stirring for 30 min. The reaction mixture was quenched with ice cold water, diluted with ethylacetate (100 mL), organic layer collected was dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford the crude. The crude was purified by column chromatography (using silica gel and 4% ethyl acetate in Hexane as eluent) to afford benzyl 1-methylcyclopropane-1-sulfonate (Int-48) (2.0 g, 93% yield). 1H NMR (300 MHz, CD3OD) δ 4.2-4.1 (2H, t), 1.7-1.6 (2H, m), 1.4 (3H, s), 1.5-1.3 (2H, m), 1.3-1.2 (2H, m), 1.0-0.9 (2H, m), 0.9 (3H, t) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394305B2
Source datasetuspto-grants-2016_07
ORD IDord-7f3b0c3eadb84975ace78d2bdbacaa7f
Source noteuspto-grants-2016_07