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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244113Generated: October 29, 2026

4-Methylthiazole → HCID 23154591, compound

https://huagongshe.com/reaction/2244113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylthiazoleHCID 12748—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(benzo[d][1,3]dioxol-5-yl)-N-methoxy-N-methylacetamideHCID 14918161—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 23154591HCID 2315459191.5%

Reaction Steps

A 2.6M solution of n-butylithium in hexane (34 ml) was dropped into a solution of 4-methylthiazole (8.0 g) of tetrahydrofuran (150 ml) at −70° C. and the mixture was stirred for 30 minutes. Further, a solution of 2-benzo(1,3)dioxol-5-yl-N-methoxy-N-methylacetamide (20.0 g) in tetrahydrofuran (20 ml) was dropped therein and the mixture was stirred for 1 hour. This solution, to which a saturated aqueous solution of ammonium chloride was added, was extracted with ethyl acetate, and after the organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated. The resultant residue was purified by silica gel flash column chromatography using a mixed solvent of ethyl acetate and hexane to yield 2-benzo(1,3)dioxol-5-yl-1-(4-methylthiazol-2-yl)ethanone (19.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678810B2
Source datasetuspto-grants-2010_03
ORD IDord-a4af4b97172f4577bbe41f5b7c45df80
Source noteuspto-grants-2010_03