HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180936Generated: October 31, 2026
1,3-Dibromopropane → HCID 12992363, compound
https://huagongshe.com/reaction/2180936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Hydrocarbostyril | HCID 64796 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12992363 | HCID 12992363 | 59.3% |
Reaction Steps
A suspension of sodium hydride (6.8 g, 60% in mineral oil) and dimethyl formamide (200 mL) was kept at 20-25° C. followed by the addition of a solution of 3,4-dihydroquinolin-2(1H)-one (25.0 g) in dimethyl formamide (180 mL). The resulting mixture was stirred at room temperature for 10 min followed by the addition of a solution of 1,3-dibromopropane (172 g) in dimethyl formamide (150 mL) at a temperature of 20-35° C. The resulting mixture was stirred at 30° C. for 20 min and concentrated in vacuo. The residue was poured onto ice, and the aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with brine, dried (MgSO4) and concentrated in vacuo. The crude product was purified by flash chromatography on silicagel (eluent:ethyl acetate/heptane 1:1) to give the product as a yellow oil (27 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06890916B2 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-aaa0ded27b7f40bdaa34ba1438250ba6 |
|---|
| Source note | uspto-grants-2005_05 |
|---|