HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520994Generated: October 29, 2026
Ammonium Chloride → HCID 58294586, compound
https://huagongshe.com/reaction/520994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 58294389 | HCID 58294389 | — |
| Reactant | HCID 178419772 | HCID 178419772 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 58294586 | HCID 58294586 | — |
Reaction Steps
Benzylzinc bromide (0.5 mol/L in tetrahydrofuran, 7.7 mL) is added to a flask charged with a stir bar, tetrakis(triphenylphosphine)palladium(0) (53 mg), and 8-bromo-5,6-dihydro-benzo[f]quinoline (0.20 g) and kept under argon atmosphere at room temperature. The resulting solution is heated to reflux temperature and stirred at this temperature for 6 h. After cooling the solution to room temperature, aqueous NH4Cl solution is added and the resulting mixture is extracted with ethyl acetate. The combined extracts are washed with brine and dried (Na2SO4). The solvent is evaporated and the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 4:1→1:1) to afford the title compound as an oil. Yield: 0.17 g (81% of theory); LC (method 1): tR=3.08 min; Mass spectrum (ESI+): m/z=272 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328072B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-17d9be26d9e34c358178b1500d78e755 |
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| Source note | uspto-grants-2016_05 |
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