HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343618Generated: October 31, 2026
Tetrabutylammonium Fluoride → HCID 86753618, compound
https://huagongshe.com/reaction/343618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86753619 | HCID 86753619 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86753618 | HCID 86753618 | 228% |
Reaction Steps
Compound 18E (23 mg, 0.0245 mmol) was dissolved in 2 ml of THF and 60 μl (0.060 mmol) of a 1M solution of nBu4NF in THF was added thereto at room temperature. After stirring for 30 minutes, the reaction mixture was diluted with ethyl acetate and washed with water. The organic layer was dried over Glauber's salt and concentrated under reduced pressure. Then the resulting residue was dissolved in 2.3 ml of THF and 100 μl of 12M hydrochloric acid was added thereto. The reaction mixture was stirred at room temperature for 1 hour and then neutralized with sodium hydrogencarbonate. After concentration, the residue was dissolved in ethanol-chloroform (1:5) and the salt was filtered off. The resulting product was purified by silica gel column chromatography (2 g of K-60 manufactured by Katayama Kagaku, eluent; methanol:chloroform=1:5). Thus 15 mg of compound 19E was obtained (yield: 99%). The properties of compound 19E were as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861520 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-0d6c998939fb4b20862b52ff13a1a428 |
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| Source note | uspto-grants-1999_01 |
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