HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Heptane | HCID 8900 | — |
| Reactant | 5-Chloro-2-(pent-4-yn-1-yl)pyrimidine | HCID 72943029 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | 3-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridine | HCID 68107814 | — |
Reaction Steps
A solution of 5-chloro-2-(pent-4-ynyl)pyrimidine (H. C. van der Plas, Tetrahedron 1989, 45, 5151-5162) (4.95 g (27.4 mmol) in nitrobenzene (50 ml) was heated to 210° C. for 1.5 hours under a continuous stream of nitrogen. The reaction was followed by TLC (silica gel, heptane: ethyl acetate=2:1; UV detection 254 nm). After completion, the reaction mixture was purified by flash chromatography on silica gel using a gradient of heptane/ethyl acetate=100:0 to 80:20 as the eluent. The 3-chloro-6,7-dihydro-5H-[1]pyrindine was obtained as a light brown solid (3.21 g, 76%); (calculated) C8H8ClN [153.61]; (found) [M+H]+=154.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242943B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-56f28acbaed341899aea456956990b81 |
| Source note | uspto-grants-2016_01 |