HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl bromoacetate → Methyl 2-(4-benzhydrylpiperazin-1-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(4-benzhydrylpiperazin-1-yl)acetate | HCID 789874 | 48% |
Reaction Steps
Methylbromoacetate (2,75 g, 18 mmol) was added dropwise to a solution of benzhydrylpiperazin (4.5 g, 18 mmol) in THF (150 ml). The reaction was stirred for 30 minutes at room temperature and a white precipitate formed. THF was removed under reduced pressure and the residue partitioned between ethyl acetate and saturated sodium bicarbonate solution. The organic layer was washed with saturated sodium bicarbonate solution and water before drying over magnesium sulphate, filtration and removal of solvent to leave (4-benzhydrylpiperazin-1-yl)-acetic acid, methyl ester as a pale brown oil (2.80 g, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753671 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-7d4dd56fbe0d4f84a76915548fe477ce |
| Source note | uspto-grants-1998_05 |