HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Methylamino)ethanol → 2-[(2-Methoxy-benzyl)-methyl-amino]-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | 1-(Bromomethyl)-2-methoxybenzene | HCID 40308 | — |
| Product | 2-[(2-Methoxy-benzyl)-methyl-amino]-ethanol | HCID 14964114 | — |
Reaction Steps
2-Methoxybenzyl bromide [J.Med. Chem., 32, 1761 (1989)] was reacted with N-methylethanolamine as described in the three previous examples to give N-(2-methoxybenzyl)-N-methylethanolamine which was reacted with 3-chloro-2-(dimethylaminomethyl)phenol in a similar manner to Example 1 (except that conversion into the dihydrochloride salt was omitted) to give the title compound b.p. 100° C. at 0.01 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05736568 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-acfde8b93412447589d6bc917f0c8cec |
| Source note | uspto-grants-1998_04 |