HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 5-methoxypyridine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Methyl 5-(benzyloxy)picolinate | HCID 15574702 | — |
| Product | Methyl 5-methoxypyridine-2-carboxylate | HCID 14282457 | — |
Reaction Steps
The following compound was prepared using benzyl bromide according to the procedure above for compound 206: Methyl 5-benzyloxypyridine-2-carboxylate (compound 207)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008487B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-71e28a5fe031452aa2e5cdaac0a752f0 |
| Source note | uspto-grants-2011_08 |