HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → (R)-3-(N-Isopropylamino)-5-methoxychroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (R)-5-methoxychroman-3-amine | HCID 10845076 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-3-(N-Isopropylamino)-5-methoxychroman | HCID 10489181 | — |
Reaction Steps
(R)-3-Amino-5-methoxychroman (1.0 g; 6mmol) and acetone (2.5 g; 40 mmol) were mixed with methanol (820 ml), acetic acid (0.4 g; 6.6 mmol) and NaCNBH3 (1.2 g; 19 mmol), pH was adjusted to 6.0 with acetic acid. Stirring was continued at room temperature for 3 days. The mixture was evaporated and the residue was made alkaline and extracted with CH2Cl2. After drying (Na2SO4) and evaporation the title compound as base was transformed to the HCl-salt. Yield: 1.1 g (83%). Mp: 289° dec. [α]D25 =-29° (C=0.015; MeOH)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420151 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-357e907a4aeb4e348d7d9c7ecfbd720e |
| Source note | uspto-grants-1995_05 |