HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Ethylpyridine → 1-(3,4-Dichlorophenyl)-3-(4-pyridyl)butane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Ethylpyridine | HCID 10822 | — |
| Reactant | 4-(2-Bromoethyl)-1,2-dichlorobenzene | HCID 15149389 | — |
| Product | 1-(3,4-Dichlorophenyl)-3-(4-pyridyl)butane | HCID 19783314 | 44.7% |
Reaction Steps
1.0 g (9.35 mmol) of 4-ethylpyridine and 2.37 g (9.35 mmol) of 3,4-dichlorophenethyl bromide were reacted in the same manner as in Example 1. The reaction product was purified to obtain 1.17 g of the desired compound (yield: 44.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05262420 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-be6104b6208b4ecb9c31f03db979c332 |
| Source note | uspto-grants-1993_11 |