HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098037Generated: October 31, 2026
Ethyl Acetate → 5-Bromo-3-(trifluoromethyl)quinoline
https://huagongshe.com/reaction/2098037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(Trifluoromethyl)quinoline | HCID 12025166 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Sodium Sulfite | HCID 24437 | — |
| Product | 8-Bromo-3-(trifluoromethyl)quinoline | HCID 46941511 | — |
| Product | 5-Bromo-3-(trifluoromethyl)quinoline | HCID 68759014 | 37% |
Reaction Steps
3-(Trifluoromethyl)quinoline (7.00 g, 35.5 mmol) and N-bromosuccinimide (9.00 g, 50.6 mmol) in concentrated sulfuric acid (50 ml) was heated to 50° C. After stirring for 1.5 h, the solution was cooled to ambient temperature, diluted with saturated aq. sodium sulfite, made alkaline with 3 N aq. sodium hydroxide, and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was flash chromatographed with 99:1, 49:1, 24:1, and 23:2 hexane:ethyl acetate as the eluant to afford 4.55 g of impure 8-bromo-3-(trifluoromethyl)quinoline and 3.89 g (37% yield) of 5-bromo-3-(trifluoromethyl)quinoline. Method [8] Retention time 6.75 and 7.47 min by HPLC (M+=276 and 278) and (M+=276 and 278).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08450363B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-2e7e3e148aca4ae9a54f369622779e32 |
|---|
| Source note | uspto-grants-2013_05 |
|---|