HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941866Generated: November 1, 2026
Tetrabutylammonium Fluoride → HCID 57475885, compound
https://huagongshe.com/reaction/1941866
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Methyl 2-(chloromethyl)oxazole-4-carboxylate | HCID 2763199 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57475885 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389513B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-36c701d6bd444d829d574b1dd89cd1ca |
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| Source note | uspto-grants-2013_03 |
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