HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzophenone → (2-Chlorophenyl)diphenylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | 1-Bromo-2-chlorobenzene | HCID 12754 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Product | (2-Chlorophenyl)diphenylmethanol | HCID 298659 | 64% |
Reaction Steps
Following the procedure outlined in Example 1, 1.3 g (52 mmol) of magnesium turnings, 10.0 g (52 mmol) of 1-bromo-2-chlorobenzene and 9.4 g (52 mmol) benzophenone gave 9.81 g (64%) of (2-Chlorophenyl) diphenyl methanol (Compound T3), mp: 91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026263B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-3ba773148c994e52aa0095ae575d3cf5 |
| Source note | uspto-grants-2011_09 |