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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736638Generated: October 29, 2026

Tetrabutylammonium Fluoride → HCID 15344101, compound

https://huagongshe.com/reaction/1736638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 10875945HCID 10875945—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15344101HCID 1534410184.4%

Reaction Steps

A solution of 74.5 mg (0.117 mmol) of (2S,3S,5S)-2-(Boc-amino)-5-(N-((3-pyridinyl)methoxycarbonyl)amino)-1-phenyl-6-(4-pyridinyl)-3-(tert-butyldimethylsilyloxy)-hexane in 4 ml of tetrahydrofuran was treated with 102 μl of 1M solution of tetrabutylammonium fluoride in tetrahydrofuran. After being stirred at ambient temperature for 24 h, the solvent was removed in vacuo, and the residue was purified by silica gel chromatography using 10% methanol in dichloromethane to provide 51.4 mg (84%) of the desired compound as a white solid. 1H NMR (CDCl3) δ1.37 (s, 9H), 1.65 (t, 2H), 2.82-3.01 (m, 5H), 3.70 (m, 2H), 4.03 (m, 1H), 4.78 (d, 1H), 5.03 (s, 2H), 5.18 (br d, 1H), 7.06 (d, 2H, 7.16-7.31 (m, 6H), 7.61 (d, 1H), 8.44 (d, 2H), 8.57 (s , 2H). Mass spectrum: (M+H)+ =521.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541321
Source datasetuspto-grants-1996_07
ORD IDord-52ff7c33e8f1493bb87a3fd47a75222a
Source noteuspto-grants-1996_07