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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023292Generated: November 3, 2026

Tetrabutylammonium Fluoride → HCID 22452057, compound

https://huagongshe.com/reaction/1023292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 23159389HCID 23159389—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22452057HCID 2245205794%

Reaction Steps

Prepared from 4-[(3-Chloro-4-fluorophenyl)amino]-7-{3-[(tert-butyl-dimethylsilyl)oxy]propyloxy}-6-nitroquinazoline by splitting off the protective silyl group with tetrabutyl ammonium fluoride in tetrahydrofuran. Yield: 94% of theory; Rf value: 0.61 (silica gel, methylene chloride/methanol/concentrated aqueous ammonia solution=90:10:0.1); mass spectrum (ESI−): m/z=391, 393 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722694B2
Source datasetuspto-grants-2014_05
ORD IDord-f831cbce005e43e5b8e851129fe2fdd9
Source noteuspto-grants-2014_05