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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65441Generated: October 26, 2026

Tetrabutylammonium Fluoride Trihydrate → Tetrabutylammonium Fluoride

https://huagongshe.com/reaction/65441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
ReactantN-p-methoxybenzyl-N-tert.-butylsulphonylmethyl-2-(S)-bromo-3-hydroxypropionic acid amideHCID 67931656—
SolventTetrahydrofuranHCID 8028—
ProductTetrabutylammonium FluorideHCID 2724141—

Reaction Steps

A solution of dehydrated tetra-n-butylammonium fluoride in tetrahydrofuran, which is prepared from tetra-n-butylammonium fluoride trihydrate by drying at 55°-60°/0.1 mm and dissolving in 40 ml of tetrahydrofuran, is added dropwise at 0° to a solution of 1.426 g (3.38 mmol) of N-p-methoxybenzyl-N-tert.-butylsulphonylmethyl-2-(S)-bromo-3-hydroxypropionic acid amide in 6 ml of tetrahydrofuran. Activated molecular sieve (4 Å) is added to the reaction mixture and the whole is stirred for 2 hours at 0°. The molecular sieve is filtered off and washed with methylene chloride; 600 ml of ether and 75 ml of buffer solution having a pH of 8 are added to the combined filtrates. After drying over sodium sulphate and concentration by evaporation in vacuo, the crude product is obtained which is purified by chromatography over 50 g of silica gel using toluene:ethyl acetate (4:1) and (2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614614
Source datasetuspto-grants-1986_09
ORD IDord-cce67ac5739e4393afc8495dd0997470
Source noteuspto-grants-1986_09