HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-((2,4-Dichlorobenzyl)(methyl)amino)-1-(4-bromophenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6,8-Dichloro-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline | HCID 22386807 | — |
| Reactant | 1-(4-Bromophenyl)-2-((2,4-dichlorobenzyl)(methyl)amino)ethanone | HCID 22386828 | — |
| Product | 2-((2,4-Dichlorobenzyl)(methyl)amino)-1-(4-bromophenyl)ethanol | HCID 22386848 | 86% |
Reaction Steps
Intermediate 1 was reduced to the corresponding alcohol with 2 equivalents of NaBH4 in analogy to the manner described for intermediate 4, example 1, and the alcohol was isolated in a yield of 86%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911453B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-4c629c70208d4be086b4f057553e5590 |
| Source note | uspto-grants-2005_06 |