HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049602Generated: November 4, 2026
1,3-Dibromopropane → HCID 131736035, compound
https://huagongshe.com/reaction/1049602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 131736036 | HCID 131736036 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131736035 | HCID 131736035 | — |
Reaction Steps
To a solution of 3-(4-((tert-butyl(dimethyl)silyl)oxy)-2′-fluoro-5′-methoxybiphenyl-2-yl)propanenitrile (165 mg) and 1,3-dibromopropane (67 μL) in THF (4 mL) was added a solution (1 M, 1.1 mL) of lithium bis(trimethylsilyl)amide in THF at 0° C., and the mixture was stirred at 0° C. for 1 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (116 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382188B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-e709d7c5d6674563a23549a8ba5215a7 |
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| Source note | uspto-grants-2016_07 |
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