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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901405Generated: October 31, 2026

Tetrabutylammonium Fluoride → HCID 15538829, compound

https://huagongshe.com/reaction/1901405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 15389177HCID 15389177—
ReactantEthyl acetate hexaneHCID 21226206—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15538829HCID 15538829—

Reaction Steps

To a solution of 0.97 g (2.78 mmol) of alkene 1a in 30 ml of dry THF was added 0.81 g (1.1 eq.) of tetra-n-butylammonium fluoride. After stirring for one hour TLC (silica, 20% ethyl acetate/hexane) showed complete conversion of starting material to a new compound. The THF was evaporated and the residue dissolved in ethyl acetate. The ethyl acetate solution was extracted four times with water and dried. Silica gel (2 g) was added and the solvent evaporated. The material was purified by column chromatography on silica gel, eluting with 10-20% ethyl acetate/hexane yielding 0.568 g (87%) of 1b: 1H NMR (CDCl3) δ 7.5-6.5 (m, 4H), 4.91 (s, 1H), 3.20 (s, 3H), 2.47 (sept, 1H), 2.33 (sept, 1H), 1.25 (d, 6H), 0.92 (d, 6H); 13C NMR (CDCl3) δ 129.25, 124.98, 122.60, 116.54, 114.98, 114.56, 56.38, 30.52, 26.80, 22.11, 21.08; Mass spectrum (m/z): 234, 219, 191; exact mass, cald'd. 234.1620, found 234.1620.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578253
Source datasetuspto-grants-1996_11
ORD IDord-496e99f8598b458892793a113713a198
Source noteuspto-grants-1996_11