HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(3-Phenylpropyloxy)benzylchloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(3-Phenylpropyloxy)benzyl alcohol | HCID 28561602 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(3-Phenylpropyloxy)benzylchloride | HCID 21841069 | 99.1% |
Reaction Steps
3.0 g of 4-(3-phenylpropyloxy)benzyl alcohol were dissolved in 30 ml of chloroform, and 1.77 g of thionyl chloride were further fed dropwise to the resultant solution. The solution was then stirred for 1 hour at room temperature. After completed the reaction, the solution reacted was poured into ice-water and extracted with chloroform. The organic layer resulted was dried with anhydrous magnesium sulfate, and the solvent used was distillated under reduced pressure, thereby affording 3.2 g of 4-(3-phenylpropyloxy)benzylchloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05965743 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-6f5d723516804e65a8cfc62df20d37b3 |
| Source note | uspto-grants-1999_10 |