HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655222Generated: October 30, 2026
6-Bromo-7-fluoroquinoline → (7-Fluoro-quinolin-6-yl)-acetic acid tert-butyl ester
https://huagongshe.com/reaction/655222
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Bromo-7-fluoroquinoline | HCID 14548343 | — |
| Reactant | HCID 178476297 | HCID 178476297 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7-Fluoro-quinolin-6-yl)-acetic acid tert-butyl ester | HCID 68534606 | 63% |
Reaction Steps
To a solution of 6-bromo-7-fluoro-quinoline (1.04 g, 4.6 mmole) in tetrahydrofuran (1 mL) was added a solution of tert-butylzincbromide acetate (20 mL, 10.4 M in tetrahydrofuran) followed by Pd(PPh3)4 (0.58 g, 0.5 mmole). The mixture was heated in a microwave reactor for 35 min at 120° C. The reaction mixture was quenched with a saturated ammonium chloride (60 mL), and extracted with ethyl acetate. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by column chromatography to afford the title compound (0.75 g, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071581B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-03ee9fde51c54e7ebdbf98d4e677d56a |
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| Source note | uspto-grants-2011_12 |
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