HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-(3-Chloromethylphenoxy)methylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Benzenemethanol, 3-(2-quinolinylmethoxy)- | HCID 14650410 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(3-Chloromethylphenoxy)methylquinoline | HCID 14501706 | — |
Reaction Steps
To a stirred solution of 14.5 g of 3-(2-quinolinylmethyloxy)benzyl alcohol in 150 ml of CHCl3 is added dropwise 7.5 ml of thionyl chloride during 10 min. The reaction mixture is stirred for 4 hours at room temperature, and then washed with NaHCO3 solution. The organic solution is separated, dried, and evaporated to give 3-(2-quinolinylmethyloxy)benzyl chloride which is used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376512B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-8276b8be418249e3a9510f9df35c4147 |
| Source note | uspto-grants-2002_04 |