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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376284Generated: October 29, 2026

Tetrabutylammonium Fluoride → HCID 10535231, compound

https://huagongshe.com/reaction/376284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 53679030HCID 53679030—
SolventTetrahydrofuranHCID 8028—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 10535231HCID 10535231—

Reaction Conditions

Temperature45 °C

Reaction Steps

3 g of 2-[6-(2-trimethylsilanyl-ethoxymethoxy-methyl)pyridin-2-yl]pyrrole-1-carboxylic acid tert-butyl ester (7.41 mmol) are added to a solution of 3 ml of 1.1 M tetrabutylammonium fluoride in tetrahydrofuran, 45 ml of tetrahydrofuran and 5 ml of hexamethylphosphoramide, containing 10 g of molecular sieve (4 angstrom). The mixture is stirred at 45° C. under argon for 8 hours. After filtration of the insoluble matter on celite, the tetrahydrofuran is evaporated off. The title product is purified by chromatography on a silica column (eluent: dichloromethane/ethyl acetate; 99:1). 0.50 g of a white solid is recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020345
Source datasetuspto-grants-2000_02
ORD IDord-aac1c4e7c53447c399817852c40b5d7d
Source noteuspto-grants-2000_02