HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(2H-3-chromenyl)-3-(N-methylpiperazino)-1-propanol hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-(2H-3-chromenyl)-3-(N-methyl-piperazino)-1-propanone hydrochloride | HCID 70597264 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(2H-3-chromenyl)-3-(N-methylpiperazino)-1-propanol hydrochloride | HCID 70595043 | — |
Reaction Steps
The hydrochloride (0.1 mole) obtained in Example 1 is dissolved in methanol (400 ml). Sodium methoxide (0.22 mole) in methanol solution is added thereto. The material is cooled to 0°-5° C. and potassium borohydride (0.4 mole) is added thereto. The material is stirred overnight. It is then evaporated in vacuo without heating, taken up into ether/H2O. The ethereal phase is washed with water, dried and evaporated, to give a pale yellow oil which is converted to the hydrochloride by addition of ethereal hydrochloric acid. M.p.=220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04181722 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-74382cc0d6f9423088f0067586cf958f |
| Source note | uspto-grants-1980_01 |