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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940035Generated: October 31, 2026

Tetrabutylammonium Fluoride Trihydrate → HCID 22880211, compound

https://huagongshe.com/reaction/1940035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
ReactantHCID 86751738HCID 86751738—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22880211HCID 22880211—

Reaction Steps

(1S,4R,5S)-6-(3,4-Dimethoxy-benzyl)-7-oxo-4-trifluoromethanesulphonyloxy-2,6-diazabicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester (1.1 g, 2.02 mmol) and tetrabutylammonium fluoride trihydrate (704 mg, 2.23 mmol) were stirred together in 10 ml of tetrahydrofuran at room temperature for 10 min. Thereafter, the solvent was removed in a vacuum, the oily residue was taken up in ethyl acetate and extracted three times with water and once with saturated aqueous sodium chloride solution. The organic phase was dried over magnesium sulphate and concentrated. The residual brown oil was chromatographed over silica gel with ethyl acetate and a pale yellow oil was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698577
Source datasetuspto-grants-1997_12
ORD IDord-70543a5e9c364924a2357f8a0e6ea627
Source noteuspto-grants-1997_12