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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029001Generated: November 3, 2026

Dimethylformamide → HCID 67325513, compound

https://huagongshe.com/reaction/1029001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
ReactantDiisopropylethylamineHCID 81531—
ReactantPropargylamineHCID 239041—
Reactant2-Bromo-3-methylbenzoic acidHCID 2735588—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventAmmonium ChlorideHCID 25517—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67325513HCID 67325513—

Reaction Steps

Thionyl chloride (0.679 mL, 9.30 mmol) was added to a solution of 2-bromo-3-methylbenzoic acid (2.0 g, 9.30 mmol) and DMF (0.072 mL, 0.930 mmol) in DCM (100 mL) at 0° C. The reaction mixture was allowed to warm to RT and stirred for 1 h and then cooled to 0° C. before DIPEA (3.25 mL, 18.60 mmol) followed by 2-propynylamine (0.766 mL, 11.16 mmol) were added. The resulting solution was stirred for 45 min at 0° C. The reaction mixture was diluted with saturated ammonium chloride and water and then extracted with EtOAc. The combined organic extracts were washed with saturated ammonium chloride, water, saturated sodium bicarbonate, saturated sodium chloride and dried over sodium sulfate. The solution was filtered and concentrated in vacuo to give the crude material as a tan solid. The crude product was dissolved in dioxane (100 mL) and cooled to 0° C. Sodium hydride (0.409 g, 10.23 mmol) was added and the mixture was stirred at RT for 30 min before bringing to a reflux. After 5 h, the reaction is concentrated. The crude material was purified by silica gel chromatography to provide 2-(2-bromo-3-methylphenyl)-5-methyloxazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-7d44f088e1c741d5ab4739ff50a8357f
Source noteuspto-grants-2014_05