HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(2-Furyl)benzyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [3-(2-Furyl)phenyl]methanol | HCID 11116545 | — |
| Product | 2-(2-Furyl)benzyl chloride | HCID 19744602 | — |
Reaction Steps
160 mg of the resulting alcohol compound was dissolved in 3 ml of anhydrous ethyl ether. Thionyl chloride (73 microliters) was added, and under ice cooling, the mixture was stirred for 3 hours. After the reaction, the reaction mixture was washed with a saturated aqueous solution of sodium chloride and 5% sodium hydrogen carbonate to give an ethyl ether solution of the captioned compound. It was used directly in the reaction of Example 58.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05234946 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-c56edbb658dd4840b4c7c5286e3f2558 |
| Source note | uspto-grants-1993_08 |