HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 13208214, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(2H-1,3-Benzodioxol-5-yl)-2-{[(2,3-dihydro-1,4-benzodioxin-2-yl)methyl]amino}ethan-1-one--hydrogen chloride (1/1) | HCID 3068441 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13208214 | HCID 13208214 | 89% |
Reaction Steps
In 15 ml of methanol is dissolved 1.0 g of 5-[2-{(1,4-benzodioxan-2-ylmethyl)amino}acetyl]-1,3-benzodioxole hydrochloride prepared according to the procedure described in Example 3 and the solution is neutralized with 2N sodium hydroxide. Thereafter, 100 mg of sodium borohydride is added and the mixture is stirred for 6 hours at room temperature. After completion of the reaction, the solvent is distilled off and the residue is dissolved in ethyl acetate and washed twice with saturated sodium chloride solution. After drying over anhydrous sodium sulfate, the solvent is distilled off and the residue is crystallized from water-alcohol to give 800 mg (89%) of 5-[2-{(1,4-benzodioxan-2-ylmethyl)amino}-1-hydroxyethyl]-1,3-benzodioxole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04684739 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-89aa6ffc9f4d4c8db3519910dae0cdda |
| Source note | uspto-grants-1987_08 |