Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 1-(Bis(4-fluorophenyl)methyl)piperazine | HCID 152932 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21689652 | HCID 21689652 | 100,783.602% |
Reaction Steps
To a mixture of epichiorohydrin (3.5 mL, 0.05 mmol) in ethanol (12 mL) at 0° C. (ice bath) and anhydrous NaH-CO3 (4.2 g, 0.05 mmol), [bis(4-fluorophenyl)methyl]piperazine (14.4 g, 0.05 mmol) in ethanol (200 mL) was added dropwise over 45 min under N2. The ice bath was removed and the mixture was allowed to come to room temperature. After 18 h the NaHCO3 was removed by filtration via a sintered glass funnel and the ethanol in the filtrate was removed in vacuo to give the crude product (21.3 g). Silica gel flash chromatography using 2.0% MeOH:CH2Cl2 gave pure product (10.05 g, 52.9%) as an amber oil. DCI/MS (M+1) 381.400 MHz 1H NMR (CDCl3)δ: 7.3 (m, 4H), 6.95 (m, 4H), 4.2 (s, 1H), 3.95 (m, 1H), 3.55 (m, 2H), 2.7 (m, 2H), 2.5 (m, 4H), 2.4 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | USRE035072 |
|---|
| Source dataset | uspto-grants-1995_10 |
|---|
| ORD ID | ord-404a6b5af046431b8364e530edd8b17d |
|---|
| Source note | uspto-grants-1995_10 |
|---|