HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoroethyl bromide → 1-(2-Fluoroethyl)-1,2,3,4-tetrahydro-7-quinolinol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoroethyl bromide | HCID 12982 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7-Quinolinol, 1,2,3,4-tetrahydro- | HCID 93980 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-Fluoroethyl)-1,2,3,4-tetrahydro-7-quinolinol | HCID 85863473 | 44% |
Reaction Steps
500 mg (3.35 mmol) 1,2,3,4-Tetrahydro-quinolin-7-ol are dissolved in 8 mL DMF and stirred at 60° C. overnight with 0.325 mL (1.3 eq) 1-bromo-2-fluoroethane, in the presence of 0.63 mL (1.1 eq) diisopropylethylamine. The reaction mixture is extracted with 0.1 N aqu. HCl and ethyl acetate. The combined organic extracts are washed with brine, dried over sodium acetate and evaporated. The residue is column chromatographed (silica gel, ethyl acetate/petroleum ether 1:2 to 1:1) to yield 290 mg (44%) desired product as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07569337B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-ea436ee646474ad3b1fcd5f35788c6be |
| Source note | uspto-grants-2009_08 |