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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65434Generated: October 25, 2026

Tetrabutylammonium Fluoride Trihydrate → HCID 18604777, compound

https://huagongshe.com/reaction/65434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
ReactantN-allyl-N-tert.-butylsulphonylmethyl-(R)-glycidic acid amideHCID 56993841—
Reactantammonium fluoride THFHCID 69831023—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18604777HCID 18604777—

Reaction Steps

A solution of 197 mg (0.757 mmol) of N-allyl-N-tert.-butylsulphonylmethyl-(R)-glycidic acid amide in 1 ml of tetrahydrofuran is introduced at 0°, with the exclusion of moisture, into 8 ml of a tetra-n-butyl; ammonium fluoride/THF solution which has been prepared from 5.0 g of tetra-n-butylammonium fluoride trihydrate by dehydrating at 60° C./0.1 torr and making up to 20 ml with tetrahydrofuran. The reaction mixture is stirred for 2 hours at room temperature and then partitioned between methylene chloride and phosphate buffer solution (pH 8.0). The crude product obtained by drying over sodium sulphate and concentration by evaporation of the organic phase is chromatographed over preparative silica gel plates using hexane/ethyl acetate (1:3). the title compound is obtained in the form of colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614614
Source datasetuspto-grants-1986_09
ORD IDord-4aba25dbbd1344a8bc8c659123e7942c
Source noteuspto-grants-1986_09