HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 54036921, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (R)-8-fluoro-5-methoxy-3-aminochroman | HCID 22871215 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54036921 | HCID 54036921 | — |
Reaction Steps
(R)-3-Amino-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran (1.62 g, 8.21 mmol) was dissolved in anhydrous methanol (20 mL) and to this was acetone (6.0 mL, 82.1 mmol) added. The reaction was cooled (ice-bath) then sodium cyanoborohydride (0.92 g, 14.8 mmol) was added, the pH was adjusted to 4-5 with acetic acid and the reaction was allowed to stir at room temperature overnight. The solvent was removed in vacuo, the remains were taken into a 2M solution of NH3 and then extracted thrice with diethyl ether. The combined ether portions were dried (MgSO4), filtered, and the solvent removed in vacuo to give the crude residue that was used as is in the next reaction. GC-MS (70 eV) M=239 (81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616610 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-39c00d1800c44318a85186ee35c4f668 |
| Source note | uspto-grants-1997_04 |