HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(4-Benzyloxy-3-chloromethylphenoxy)-5-methyl-7-nitroindane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [2-Benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)phenyl]methanol | HCID 23031098 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(4-Benzyloxy-3-chloromethylphenoxy)-5-methyl-7-nitroindane | HCID 23031167 | — |
Reaction Steps
[2-benzyloxy-5-(5-methyl-7-nitroindan-4-yloxy)phenyl]methanol (2.48 g) was dissolved in diethyl ether. After adding dropwise thionyl chloride (5 mL) under ice-cooling with stirring, the mixture was stirred at room temperature for 6 hours. The reaction mixture was evaporated under reduced pressure to dryness. After adding water (10 mL), the residue was extracted with diethyl ether. The organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give the title compound (2.04 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230031B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-0580df68c11b4842a5f286b946988595 |
| Source note | uspto-grants-2007_06 |