HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Ethylpyridine → 1-(3-Chlorophenyl)-3-(4-pyridyl)-butane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Ethylpyridine | HCID 10822 | — |
| Reactant | 1-(2-Bromoethyl)-3-chlorobenzene | HCID 140140 | — |
| Product | 1-(3-Chlorophenyl)-3-(4-pyridyl)-butane | HCID 19783364 | 28.3% |
Reaction Steps
1.0 g (9.35 mmol) of 4-ethylpyridine and 2.05 g (9.35 mmol) of 3-chlorophenethyl bromide were reacted in the same manner as in Example 1. The reaction product was purified to obtain 0.65 g of the desired compound (yield: 28.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05262420 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-b44d2b926edc42f4a93bced206e96fe7 |
| Source note | uspto-grants-1993_11 |