HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,6-dimethyl-4-[N-methyl-N-(1-phenyl-1H-pyrazol-3-yl) amino]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2,6-dimethyl-4-(1-phenyl-1H-pyrazol-3-yl) aminophenol | HCID 19927913 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,6-dimethyl-4-[N-methyl-N-(1-phenyl-1H-pyrazol-3-yl) amino]phenol | HCID 54032820 | — |
Reaction Steps
To 2,6-dimethyl-4-(1-phenyl-1H-pyrazol-3-yl)amino phenol (8 g), acetic acid (2.8 ml), and aqueous 40% formaldehyde (3.1 ml) in acetonitrile (40 ml) was added sodium cyanoborohydride (5.4 g). After 2 hours the mixure was quenched with water and extracted with dichloromethane. The organic phase was washed with aqueous sodium bicarbonate solution, then water, dried, evaporated and chromatographed (silica, dichloromethane) to give the title product (3 g), mp 139°-140° (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428044 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-84a8aa784eb9465c874d65b7ee256831 |
| Source note | uspto-grants-1995_06 |