HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21996975, compound → HCID 21996970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21996975 | HCID 21996975 | — |
| Reactant | HCID 21996981 | HCID 21996981 | — |
| Product | HCID 21996970 | HCID 21996970 | — |
Reaction Steps
Employing the same general procedure as for the 5-bromo-2-hydroxy-4′-methylbenzophenone (Compound K), 319 mg (1.0 mmol) of 5-bromo-2-methoxy-4-methyl-4′-methylbenzophenone (Compound I) was converted into the title compound using 2.4 mL (2.4 mmol) of boron tribromide (1M in dichloromethane) and 10 mL of dichloromethane. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) gave the title compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235923B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-6de7745f09114e20bd712769e7e53a65 |
| Source note | uspto-grants-2001_05 |