HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21996968, compound → HCID 21996988, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21996968 | HCID 21996968 | — |
| Reactant | HCID 21996975 | HCID 21996975 | — |
| Product | HCID 21996988 | HCID 21996988 | — |
Reaction Steps
Employing the same general procedure as for the preparation 5-bromo-2-hydroxy-4′-methylbenzophenone (Compound K), 533 mg (1.7 mmol) of 5-bromo-2-methoxy-3′-methylbenzophenone (Compound J) was converted into the title compound using 2.6 mL (2.6 mmol) of boron tribromide (1M in dichloromethane) and 15 mL of dichloromethane. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) gave the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06225494B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-e0e682dfb3aa442bbeffb9f1fb04c9a9 |
| Source note | uspto-grants-2001_05 |