HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidineheptanoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl 7-bromoheptanoate | HCID 122490 | — |
| Reactant | Bis(4-fluorophenyl)(piperidin-4-yl)methanol | HCID 11208889 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[Bis(4-fluorophenyl)hydroxymethyl]-1-piperidineheptanoic acid ethyl ester | HCID 54069066 | 87% |
Reaction Steps
This compound was prepared according to the procedure used in Example 7. A mixture of 4.6 g (0.015 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 3.6 g (0.015 mole) of ethyl 7-bromoheptanoate, 6.4 g (0.061 mole) of anhydrous sodium carbonate and 0.3 g (0.002 mole) of potassium iodide in 50 ml of N,N-dimethylformamide gave 6.0 g of a dark oil. The oil was purified by high pressure liquid chromatography (Waters Associates Prep LC/System 500A; PrepPAK® 500/silica; ethyl acetate; flow rate 150 ml/min). The fractions containing the desired product were combined and concentrated under reduced pressure to yield 2.5 g (44%) of a viscous, yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05057524 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-9c7064914503495f89defc295b079e3a |
| Source note | uspto-grants-1991_10 |