HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3-Bromo-alpha-hydroxybenzyl)-3-methoxymethoxypyridine 1-oxide → 2-(3-Bromobenzoyl)-3-methoxymethoxy pyridine 1-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3-Bromo-alpha-hydroxybenzyl)-3-methoxymethoxypyridine 1-oxide | HCID 54223976 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3-Bromobenzoyl)-3-methoxymethoxy pyridine 1-oxide | HCID 54465689 | 94.2% |
Reaction Steps
A suspension of 2-(3-bromo-α-hydroxybenzyl)-3-methoxymethoxypyridine 1-oxide (4.58 g) and activated manganese dioxide (13.1 g) in ethyl acetate (150 mL) was stirred overnight at room temperature. The reaction mixture was subjected to filtration, and the filtrate was concentrated under reduced pressure. The concentrate was purified by means of a silica gel column (ethyl acetate--hexane) to afford 2-(3-bromobenzoyl)-3-methoxymethoxy pyridine 1-oxide (4.29 g). Physical properties and spectrum data of the product are shown below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891895 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-d13c71dc392b4491977924931e22e7da |
| Source note | uspto-grants-1999_04 |