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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875225Generated: October 30, 2026

Hydrochloric Acid → HCID 66887902, compound

https://huagongshe.com/reaction/875225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Bromo-1-methyl-1H-imidazoleHCID 1515258—
ReactantN-methoxy-N-methylthiophene-3-carboxamideHCID 22489894—
ReactantHCID 178418443HCID 178418443—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66887902HCID 6688790251.6%

Reaction Steps

To a solution of 5-Bromo-1-methyl-imidazole (18.8 g, 117 mmol) in dichloromethane (50 mL) was added dropwise ethylmagnesium bromide (3 M in Et2O, 38.9 mL, 117 mmol). After stirring at room temperature for 30 min, the reaction mixture was cooled down to 0° C. with an ice-brine bath and N-methoxy-N-methylthiophene-3-carboxamide (20.0 g, 117 mmol) was added dropwise. The mixture was stirred for 3.5 h at room temperature. The mixture was worked-up by addition of water (400 mL), then acidified with aq. HCl (1 M) until pH=7. After extraction with dichloromethane (3×100 mL), the organic layers were washed with water (100 mL) then dried over MgSO4 and concentrated in vacuo. Purification of the residue on silica gel afforded (1-methyl-1H-imidazol-5-yl)(3-thienyl)methanone [11.6 g, yield 41%; HPLC/MS: m/z=193 (M+H); log P(HCOOH)=0.43].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981111B2
Source datasetuspto-grants-2015_03
ORD IDord-e73ac6507803498c800490ffdf6c8303
Source noteuspto-grants-2015_03