HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 2-Naphthol, 6-bromo-1-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Reactant | 6-Bromo-1-chloronaphthalen-2-ol | HCID 22048159 | — |
| Product | 2-Naphthol, 6-bromo-1-methyl- | HCID 27977 | — |
Reaction Steps
Preparation of 6-bromo-1-chloro-2-naphthol 4 from the corresponding 6-bromo-2-naphthol 3 is described in the literature (Buu-Hoi, JOC 1951, 16, 185), Scheme II. 6-Bromo-1-methyl-2-naphthol 7 was prepared as depicted in reaction Scheme II. Reaction of 6-bromo-2-naphthol 3 with aqueous dimethyl amine and aqueous formaldehyde in alcohol afforded the Mannich product 5. Reaction of 5 with acetyl chloride in methylene chloride or chloroform afforded the acetate 6. Hydride reduction of 6 in a solvent such as ethanol followed by basic work-up yielded the desired 6-bromo-1-methyl-2-naphthol 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06599925B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-92c5e4bd17bb4eebb98e4fe4a06b8f0b |
| Source note | uspto-grants-2003_07 |