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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891592Generated: October 30, 2026

Tetrabutylammonium Fluoride → HCID 22242765, compound

https://huagongshe.com/reaction/891592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 22242932HCID 22242932—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22242765HCID 2224276576.2%

Reaction Steps

To a solution of 3-t-butyldiphenylsilyloxy-1-(4-carbamoyl-1,3-oxazol-2-yl)azetidine (1.30 g, 3.08 mmol) in tetrahydrofuran (60 ml) was added a solution of 1.0M tetra-n-butylammonium fluoride in tetrahydrofuran (3.1 ml) in an ice bath, and the mixture was stirred for 1 hour. After checking the completion of the reaction, the reaction mixture was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using ethyl acetate:methanol (10:1) as the eluant to afford 1-(4-carbamoyl-1,3-oxazol-2-yl)-3-hydroxyazetidine (0.43 g, yield 75%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-f1d302031e4842ce91dacbbe578afc54
Source noteuspto-grants-2006_02