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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067292Generated: November 4, 2026

Tetrabutylammonium Fluoride → HCID 21192932, compound

https://huagongshe.com/reaction/1067292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 21192931HCID 21192931—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 21192932HCID 2119293256.3%

Reaction Steps

N-(2-(2-Tert-butyldimethylsilyloxyethyl)-8-chloro-1,2,3,4-tetrahydroisoquinolin-7-yl)-4-methoxy-3-trifluoromethylbenzamide (0.09 g) in tetrahydrofuran (10 ml) was treated with tetrabutylammonium fluoride in tetrahydrofuran (1M, 0.16 ml) at room temperature overnight. The reaction mixture was diluted with ethyl acetate, washed with water, the organic phase dried (MgSO4) and solvent removed at reduced pressure. The residue was column chromatographed (silica gel, ammonia/methanol/dichloromethane mixtures as eluant) to give the title compound (0.04 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248754B1
Source datasetuspto-grants-2001_06
ORD IDord-085c965a3c0f477393df59a5dc721623
Source noteuspto-grants-2001_06