HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829806Generated: November 2, 2026
Tetrabutylammonium Fluoride → HCID 10295484, compound
https://huagongshe.com/reaction/1829806
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 10186857 | HCID 10186857 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10295484 | HCID 10295484 | 62.3% |
Reaction Steps
To an ice cooled solution of 1-[(2S,3R)-5-(6-bromo-2-naphthyloxy)-2-(tert-butyldimethylsilyloxy)-3-pentyl]imidazole-4-carboxamide (120 mg, 0.225 mmol) in THF (5 ml) was added dropwise 1.0 M tetra-n-butylammonium fluoride in THF (338 μl). After the addition was completed, the reaction mixture was stirred at ice-bath temperature for 2 hours. The reaction was quenched by addition of 25% aqueous AcONH4 (5 ml) and H2O (10 ml) The resulting mixture was stirred for several minutes and then extracted with ethyl acetate (30 ml). The organic layer was washed with brine, dried (sodium sulfate) and concentrated under reduced pressure. The residue was purified by silica gel (4 g) column chromatography eluting with chloroform/methanol (100:1 to 20:1) to give 1-[(2S,3R)-5-(6-bromo-2-naphthyloxy)-2-hydroxy-3-pentyl]imidazole-4-carboxamide (16) (58.6 mg, 62.2%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07064144B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-867abbd730bb4ff8983a4c6a90dc1bf8 |
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| Source note | uspto-grants-2006_06 |
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