HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Benzyloxy)-5-bromobenzaldehyde → HCID 4722225, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Benzyloxy)-5-bromobenzaldehyde | HCID 733087 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Product | HCID 4722225 | HCID 4722225 | — |
Reaction Steps
In a manner similar to that of Example 75(b), by reacting 22.5 g (77 mmol) of 2-benzyloxy-5-bromobenzaldehyde, 26.1 g (386 mmol) of methylamine hydrochloride and 7.3 g (116 mmol) of sodium cyanoborohydride, and after purification by chromatography on a column of silica eluted with a dichloromethane/methanol mixture (9/1) and 0.5% isopropylamine, 12.2 g (51%) of the expected product are obtained in the form of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06927228B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-5269bcc013af439b92b9f196d8aefa7e |
| Source note | uspto-grants-2005_08 |