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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791006Generated: November 4, 2026

1-(methoxymethyl)-1H-imidazole → HCID 22042653, compound

https://huagongshe.com/reaction/1791006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(methoxymethyl)-1H-imidazoleHCID 88359—
ReactantHCID 22042580HCID 22042580—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22042653HCID 22042653—

Reaction Steps

To a solution of 55 mg (0.49 mmol) of 1-methoxymethyl-1H-imidazole in 5 ml of THF at −78° C. was added 0.20 ml (0.50 mmol) of a 2.5 M solution of n-butyllithium in hexanes and the resultant mixture was stirred at −78° C. for 30 mins. After this time, a solution of 160 mg (0.47 mmol) of N-methyl-N-(4-trifluoroacetyl-phenyl)-benzenesulfonamide (Example 22, Step A) in 2 ml of THF was added and the resultant mixture stirred at −78° C. for a further 2 h, and then at room temperature for 14 h. After this time the reaction was quenched by the addition of a saturated aqueous solution of ammonium chloride and extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica gel (hexanes:EtOAc, 4:1) to give the title compound. 1H-NMR (CDCl3) δ 3.09 (s, 3H), 3.19 (s, 3H), 4.90 (s, 2H), 5.16 (brs, 1H), 7.07–7.16 (m, 4H), 7.42–7.62 (m, 7H). Mass Spectrum (CI+) m/e=456.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071358B2
Source datasetuspto-grants-2006_07
ORD IDord-068cd57809ed447eb08a6bef3d7309e1
Source noteuspto-grants-2006_07