HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643269Generated: November 2, 2026
Ammonium Chloride → (3S,5R)-3-((E)-but-2-enyl)-5-(4-fluorophenyl)dihydrofuran-2(3H)-one
https://huagongshe.com/reaction/1643269
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Butene, 1-bromo- | HCID 122414 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (R)-5-(4-fluorophenyl)dihydrofuran-2(3H)-one | HCID 7020398 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | (3S,5R)-3-((E)-but-2-enyl)-5-(4-fluorophenyl)dihydrofuran-2(3H)-one | HCID 59568805 | — |
Reaction Steps
To the solution of lithium bis(trimethylsilyl)amide (2.4 mL, 2.4 mmol, 1M in THF) in anhydrous 20 mL THF at −70° C. was slowly added over 15 minutes (R)-5-(4-fluorophenyl)dihydrofuran-2(3H)-one (360 mg, 2.0 mmol) as a solution in 1.0 mL THF. The reaction mixture was stirred for 20 min at −70° C. and then for 10 min at room temperature. The mixture was cooled to −70° C. and to it was slowly added a pre-cooled solution of 1-bromo-but-2-ene (324 mg, 2.4 mmol) in 400 μl HMPA an 100 μL of THF. The resulting mixture was stirred at −70° C. for 2 h and the temperature was slowly raised over a period of 2 h. The mixture was poured into 20 mL saturated NH4Cl and extracted with ethyl acetate (3×30 mL). The combined organic layers were washed with brine (2×20 mL) and dried over Na2SO4. The solvent was removed under reduced pressure and the product isolated by Flash column chromatography eluting with 0% to 50% ethyl acetate/hexane to the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119692B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-7bbb1d34b20f4b35a164b20c51ecf1f0 |
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| Source note | uspto-grants-2012_02 |
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