HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 3-benzylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Product | 3-benzylthiophene | HCID 10487471 | 74% |
Reaction Steps
3-benzylthiophene was prepared in the same manner as described in Example 32C using 3-thienylboronic acid and benzyl bromide, 74% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962490 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-c82cc84378aa48e3bf2d8b20d09ec4da |
| Source note | uspto-grants-1999_10 |