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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670336Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 59852950, compound

https://huagongshe.com/reaction/1670336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantCarbamic acid, [6-[(trimethylsilyl)ethynyl]-3-pyridinyl]-, 1,1-dimethylethyl esterHCID 59853054—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59852950HCID 59852950100%

Reaction Steps

A solution of tert-butyl 6-(2-(trimethylsilyl)ethynyl)pyridin-3-ylcarbamate (62 mg, 0.21 mmol) in THF (5 mL) was cooled to −15° C. and treated with 1.0 M tetrabutylammonium fluoride (Aldrich, 0.25 mL, 0.25 mmol) and stirred for 40 min. The mixture was concentrated in vacuo and partitioned between EtOAc and saturated aqueous NaHCO3 solution. The EtOAc phase was washed with brine, dried (MgSO4) and concentrated in vacuo to give the title compound (45 mg, 100%) as an off-white solid. 1H NMR (DMSO-d6) δ 9.78 (s, 1H), 8.58 (d, 1H, J=2.5 Hz), 7.92-7.84 (m, 1H), 7.46 (d, 1H, J=8.6 Hz), 4.17 (s, 1H), 1.47 (s, 9H); MS (ESI+): m/z 219.20 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989477B2
Source datasetuspto-grants-2011_08
ORD IDord-5299794fb30c4b848f6fd9dbc2b55510
Source noteuspto-grants-2011_08