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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743257Generated: November 4, 2026

Tetrabutylammonium Fluoride → HCID 58604483, compound

https://huagongshe.com/reaction/1743257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 58604471HCID 58604471—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58604483HCID 58604483—

Reaction Conditions

Temperature0 °C

Reaction Steps

337 mg of methyl (3R,6S,7aS)-6-tert-butoxycarbonylamino-6-(tert-butyldimethylsilanyloxymethyl)-5-oxohexahydropyrrolo[2,1-b]thiazole-3-carboxylate were dissolved in 10 ml of THF and cooled to 0° C. A 1 M solution of tetrabutylammonium fluoride was added dropwise, and the mixture was allowed to reach room temperature within 2 h. It was then partitioned between 120 ml of saturated ammonium chloride solution and 120 ml of ethyl acetate. The aqueous phase was extracted twice with 40 ml of ethyl acetate each time. The combined organic phases were washed once with 80 ml of saturated sodium chloride solution and dried with MgSO4. The solvents were removed in vacuo, and the residue was purified by chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008957B2
Source datasetuspto-grants-2006_03
ORD IDord-1ada77661afc4138aa38c9616c970e7e
Source noteuspto-grants-2006_03