HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 178508043, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 21941354 | HCID 21941354 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178508043 | HCID 178508043 | — |
Reaction Steps
The mixture of 5-methoxy-4-p-nitrobenzyloxycarbonyl-1,2,3,6-tetrahydropyrazine (5.7 g) and ammonium chloride (1.6 g) in dry ethanol (100 mL) was heated to reflux for 4 hours. The reaction mixture was then concentrated under reduced pressure. Dichloromethane (100 mL) was added to the residue and extracted with water (3×50 mL) then the combined aqueous layer was washed with dichloromethane. The aqueous layer was neutralized with 10% potassium carbonate aqueous solution and then extracted with dichloromethane (8×50 mL). The combined organic layer was dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure and the title compound was obtained as a white solid. Yield: 4.9 g, 91.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112582B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-0e196c8edeac44c7a16ace1e376df424 |
| Source note | uspto-grants-2006_09 |