HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351665Generated: October 25, 2026
Boron trifluoride etherate → HCID 21099443, compound
https://huagongshe.com/reaction/1351665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 4-(Benzenesulfonyl)benzaldehyde | HCID 14417477 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Reactant | HCID 178505764 | HCID 178505764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21099443 | HCID 21099443 | 90% |
Reaction Steps
Lithium chloride (0.57 g, 13.5 mmol, dried at 140° C. under vacuum) and copper(I) cyanide (0.605 g, 6.8 mmol) were dissolved in tetrahydrofuran (5 mL) and cooled to −40° C. under nitrogen. 4-Fluorobenzylzinc chloride (0.5M in tetrahydrofuran, 15 mL) was added dropwise and the solution cooled to −20° C. for 5 minutes then to −78° C. Boron trifluoride diethyl etherate (1.7 mL, 13.5 mmol) and 4-(phenylsulfonyl)benzaldehyde (Example 113 Step 1, 300 mg, 1.2 mmol) in tetrahydrofuran (5 mL) were added and the reaction stirred at −78° C. for 30 minutes then warmed to 25° C. and quenched with saturated ammonium chloride solution. Ethyl acetate was added and the mixture stirred for 10 minutes then the layers separated. The organic layer was washed with brine, dried over MgSO4 and evaporated. The residue was purified by flash column chromatography on silica, eluting with 40% ethyl acetate/isohexane, to give the title compound as a white solid (0.386 g, 90%). δH (360 MHz, CDCl3): 7.94–7.88 (4H, m), 7.58–7.43 (5H, m), 7.10–7.02 (2H, m), 6.99–6.93 (2H, m), 4.92–4.88 (1H, m), 2.99–2.85 (2H, m), 2.01 (1H, d, J=3.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217740B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-8129b47305a5431d845f5b63c57ff080 |
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| Source note | uspto-grants-2007_05 |
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