Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54250348 | HCID 54250348 | 119.1% |
Reaction Steps
Sodium triacetoxyborohydride (27.9 g, 134 mmol) is added portionwise over 45 minutes to a 0° C. solution of 2-methoxyaniline (12.5 g, 101 mmol) in THF (100 mL), acetone (7.82 mL, 106 mmol) and acetic acid (5.9 mL) and the resultant mixture is allowed to attain RT overnight. The reaction mixture is cooled to 0° C. and then water (50 mL) is added slowly followed by 50% aqueous sodium hydroxide solution (20 mL) and the resultant mixture stirred for 1.5 h. The organics were removed and the residual aqueous phase diluted with water (30 mL) and extracted into ethyl acetate (3×50 mL). The combined organics were washed with water (2×100 mL), brine (50 mL), dried (MgSO4) and concentrated in vacuo to afford N-Isopropyl-N-(2-methoxy-phenyl) aniline (14.51 g) as an amber oil which is used without further purification: 1H NMR (300 MHz, CDCl3) δ6.91 (t, 1H, J=7.6), 7.01 (d, 1H, J=7.6), 6.68 (t, 2H, J=7.9), 3.88 (s, 3H), 3.66 (m, 1H, J=6.8), 1.28 (d, 6H, J=6.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05859007 |
|---|
| Source dataset | uspto-grants-1999_01 |
|---|
| ORD ID | ord-6eb44edc23d84c5aaf47dee198ca67b2 |
|---|
| Source note | uspto-grants-1999_01 |
|---|