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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941866Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 57475885, compound

https://huagongshe.com/reaction/1941866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 2-(chloromethyl)oxazole-4-carboxylateHCID 2763199—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 57475885HCID 57475885—

Reaction Steps

A solution of methyl 2-(chloromethyl)oxazole-4-carboxylate (CAS208465-72-9) (150 mg, 0.85 mmol) in acetonitrile (4.27 ml) was treated with tetra-n-butylammonium fluoride (2.56 ml, 2.56 mmol). The blue solution turned to orange and was left under stirring at room temperature overnight. For the workup, the reaction mixture was poured in water and extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulphate, and concentrated at reduced pressure. The crude material was purified by chromatography on a flash NH2 column using a gradient of heptane/ethyl acetate=100/0 to 50/50 as the eluent. The 2-fluoromethyl-oxazole-4-carboxylic acid methyl ester was obtained as a white solid (64 mg, 47% of theory). MS (ISP): m/z=160.1 [M+H]+. b) 2-Fluoromethyl-oxazole-4-carboxylic acid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389513B2
Source datasetuspto-grants-2013_03
ORD IDord-36c701d6bd444d829d574b1dd89cd1ca
Source noteuspto-grants-2013_03