HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → 2-Amino-5-bromobenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Product | 2-Amino-5-bromobenzophenone | HCID 99677 | 19.8% |
Reaction Steps
The procedure was in the same manner as described in example 15, except that the starting material was benzoic acid instead of p-chlorobenzoic acid and 4-bromoaniline instead of 4-chloroaniline. The title compound was obtained as yellow needle crystal, and yield 19.8%, m.p.109-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06960611B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-2c535ab9358a45d38e9c976d4d01f759 |
| Source note | uspto-grants-2005_11 |