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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732872Generated: October 29, 2026

N-methoxy-N-methyl-2-(thiophen-2-yl)acetamide → 1-[4-(1-Azido-1-methylethyl)phenyl]-2-(2-thienyl)ethanone

https://huagongshe.com/reaction/732872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methoxy-N-methyl-2-(thiophen-2-yl)acetamideHCID 15029898—
Reactant1-(1-Azido-1-methylethyl)-4-bromobenzeneHCID 53838962—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(1-Azido-1-methylethyl)phenyl]-2-(2-thienyl)ethanoneHCID 86617463—

Reaction Steps

nBuLi (1.6M in hexane, 2.88 mL, 4.60 mmol) was added dropwise to a solution of 1-(1-azido-1-methylethyl)-4-bromobenzene (2-3, 1.03 g, 4.28 mmol) in THF (20 mL) at −78° C. After 15 min a solution of N-methoxy-N-methyl-2-thien-2-ylacetamide (1-1, 0.78 g, 4.18 mmol) in THF (1 mL) was added. After an additional 30 min at −78° C., the reaction was quenched with saturated ammonium chloride solution and extracted with ethyl acetate, dried over magnesium sulfate, filtered, and concentrated to give an oil. The crude product was purified via automated flash column chromatography on silica gel (5% CH2Cl2, 0-10% EtOAc/hexanes over 30 min) to give the title compounds as a yellow oil. LRMS m/z (M+1) Calcd: 286.1,. Found 286.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589068B2
Source datasetuspto-grants-2009_09
ORD IDord-a3f13adaa5db48cdb95bb1e17ae7bac1
Source noteuspto-grants-2009_09