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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918825Generated: November 2, 2026

Dimethylformamide → HCID 67016364, compound

https://huagongshe.com/reaction/1918825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant4-nitro-1H-pyrazoleHCID 16376—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67016364HCID 6701636492.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

A 100-mL single-neck round-bottomed flask equipped with a reflux condenser and magnetic stirrer was purged with nitrogen and charged with 4-nitro-1H-pyrazole (500 mg, 4.42 mmol), (2-bromoethoxy)(tert-butyl)dimethylsilane (2.12 g, 8.85 mmol), cesium carbonate (5.76 g, 17.7 mmol) and anhydrous DMF (5 mL). After heating at 70° C. for 1 h, the mixture was cooled to room temperature and diluted with methylene chloride (50 mL) and water (30 mL). The organic layer was separated, and the aqueous layer was extracted with methylene chloride (2×30 mL). The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography to afford a 92% yield (1.11 g) of 116a as a white solid: mp 63-64° C.; 1H NMR (500 MHz, CDCl3) d 8.20 (s, 1H), 8.08 (s, 1H), 4.24 (t, 2H, J=4.5 Hz), 3.95 (t, 2H, J=4.5 Hz), 0.84 (s, 9H), −0.04 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618107B2
Source datasetuspto-grants-2013_12
ORD IDord-8cd6c2aa72cc4282af444243d7710e56
Source noteuspto-grants-2013_12