HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride, 3-nitro- → (4-Methylpiperazin-1-yl)(3-nitrophenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride, 3-nitro- | HCID 8495 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Methylpiperazin-1-yl)(3-nitrophenyl)methanone | HCID 763411 | 86% |
Reaction Steps
To a solution of 3-nitrobenzoyl chloride (4.5 g, 24.25 mmol) in THF (30 ml) was added 1-methylpiperazine (8.50 g, 85 mmol). The reaction was stirred for 20 min at room temperature. The reaction mixture was diluted with 50 mL water and extracted with ethyl acetate (2×100 mL). The combined organic layer was washed with brine (50 mL). The brine was back extracted with ethyl acetate (2×50 mL) and all the organic layers were combined, dried over magnesium sulphate, filtered, and concentrated under vacuum give the title product (5.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428499B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-527177e999374add81098adf56dd4054 |
| Source note | uspto-grants-2016_08 |