HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-formylphenylboronic acid → 4-Chloro-2-formylphenylboronic Acid (contains varying amounts of Anhydride)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-formylphenylboronic acid | HCID 3806952 | — |
| Reactant | HCID 58244852 | HCID 58244852 | — |
| Product | 4-Chloro-2-formylphenylboronic Acid (contains varying amounts of Anhydride) | HCID 23730425 | 70% |
Reaction Steps
The title compound 24a was synthesized following the 2-step procedure reported for the synthesis of 10-tert-butyl 6-methyl 3-chloro-13-cyclohexyl-7H-indolo[2,1-a][2]benzazepine-6,10-dicarboxylate 21a, using 5-chloro-2-formylphenylboronic acid in the first step, instead of 4-chloro-2-formylphenylboronic acid 34a, and was obtained with an overall yield of 70% as a yellowish solid; m/z 507 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09427440B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-38e5239fe34d4e88a6697eaa90dc0395 |
| Source note | uspto-grants-2016_08 |