HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 4-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzoyl chloride, 3,4,5-trimethoxy- | HCID 78282 | — |
| Reactant | Methyl Piperazine-2-carboxylate Dihydrochloride | HCID 2760425 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate | HCID 20066647 | 60.2% |
Reaction Steps
A solution of 3,4,5-trimethoxybenzoyl chloride (10.9 g) in dichloromethane (100 ml) is added dropwise taking one hour, under ice-cooling while stirring, to a mixture of methyl piperazine-2-carboxylate dihydrochloride (10.24 g), triethylamine (18.7 g) and dichloromethane (200 ml). The reaction mixture is poured into ice-water, followed by extraction with dichloromethane. The organic layer is washed with water, dried and the solvent is distilled off under reduced pressure. Crystals obtained from the residue are recrystallized from ethyl acetate and hexane to afford methyl 4-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate (9.6 g) as colorless needles, m.p. 113-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997836 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-b823256a481d4700b5ccad7bb1278d79 |
| Source note | uspto-grants-1991_03 |