HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743257Generated: November 4, 2026
Tetrabutylammonium Fluoride → HCID 58604483, compound
https://huagongshe.com/reaction/1743257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 58604471 | HCID 58604471 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58604483 | HCID 58604483 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07008957B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-1ada77661afc4138aa38c9616c970e7e |
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| Source note | uspto-grants-2006_03 |
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