HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → (E)-4-(4-chloro-1-butenyl)isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (E)-4-(4-isoquinolinyl)-3-buten-1-ol | HCID 14750832 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (E)-4-(4-chloro-1-butenyl)isoquinoline | HCID 14750833 | — |
Reaction Steps
A solution of 3.3 g of (E)-4-(4-isoquinolinyl)-3-buten-1-ol in 15 mL of dry chloroform was added to a cold solution of 1.8 mL of thionyl chloride in 5 mL of dry chloroform. After 15 minutes, the cooling bath was removed and the reaction was stirred at room temperature for 1 hour and then at reflux for 3 hours. The cooled mixture was washed with NaHCO3 solution and with brine then was dried (Na2SO4) and evaporated. The residue was purified by chromatography over silica gel (ethyl acetate-toluene; 3:17) to yield 2.2 g of (E)-4-(4-chloro-1-butenyl)isoquinoline as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04916145 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-8739ed825a2f4ea1a068edbe08a91bca |
| Source note | uspto-grants-1990_04 |