HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → (2-Chlorophenyl)(4-chlorophenyl)methyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2-Chlorophenyl)(4-chlorophenyl)methanol | HCID 247332 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (2-Chlorophenyl)(4-chlorophenyl)methyl chloride | HCID 247330 | 102.3% |
Reaction Steps
A stirred solution of 9.0 grams (0.036 mole) of (2-chlorophenyl)(4-chlorophenyl)methanol in 90 mL of chloroform was cooled to 0° C., and 5.3 mL (0.072 mole) of thionyl chloride was added. Upon completion of the addition the reaction mixture was allowed to warm to ambient temperature, where it stirred for about 18 hours. After this time the reaction mixture was filtered and concentrated under reduced pressure. The filtrate was taken up in hexane and subjected to column chromatography on silica gel with hexane as eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 10.0 grams of (2-chlorophenyl)(4-chlorophenyl)methyl chloride. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USH0002007H1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-a81c024108954c3da6b384adb0a4da93 |
| Source note | uspto-grants-2001_12 |