HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170439Generated: October 30, 2026
1,3,5-Trifluorobenzene → HCID 178464146, compound
https://huagongshe.com/reaction/1170439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3,5-Trifluorobenzene | HCID 9745 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 178464130 | HCID 178464130 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178464146 | HCID 178464146 | 27.2% |
Reaction Steps
A solution of 1,3,5-trifluorobenzene (318 mg, 2.41 mmol) in tetrahydrofuran (6.0 mL) was cooled to 78° C. under nitrogen, and thereto was added dropwise 2N lithium diisopropylamide (1.53 mL, 3.06 mmol), and the mixture was stirred for 30 minutes, Then, thereto was added dropwise a solution of the compound of Example 1-1 (650 mg, 1.34 mmol) in tetrahydrofuran (16 mL), and the mixture was stirred at −78° C. for 3 hours. To the reaction solution was added saturated aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate, dried over magnesium sulfate and filtered. The filtrate was evaporated and purified by silica gel column chromatography (hexane/ethyl acetate/ammonia water=50/1/0.25 to 30/1/0.16 to 20/1/0.1) to give the titled compound (223 mg, 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825155B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-06835bc7a0934ab083bc7caceb71ca91 |
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| Source note | uspto-grants-2010_11 |
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