HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747483Generated: October 30, 2026
Ethyl Acetate → 3-fluoro-6-methoxyquinoline
https://huagongshe.com/reaction/747483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 11737373 | HCID 11737373 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-fluoro-6-methoxyquinoline | HCID 11309840 | 100.2% |
Reaction Steps
A suspension of 1007 g of 6-methoxy-3-quinolinediazonium fluoroborate taken in 9 l of toluene is heated to 60° C. in 85 minutes. A release of gas is observed at 60° C. The reaction medium is then gradually heated further for 90 minutes to 70-72° C. After having been kept at 72° C. for 90 minutes, the medium is then gradually heated again to 85° C. After cooling and stirring overnight, 4 l of ice-cold water are added to the suspension. After having stirred for 15 minutes, 2.5 l of ethyl acetate are added. After having stirred for 45 minutes, the pH is adjusted to pH=7-7.5 by adding 47% sodium hydroxide (250 ml). The medium is stirred for 30 minutes and then separated by settling out for 1 hour. The lower aqueous phase is re-extracted with ethyl acetate. The organic phases are combined together and washed with water. The solution is filtered and then concentrated under reduced pressure so as to give 655 g of crude 3-fluoro-6-methoxyquinoline. The crude product is distilled under reduced pressure. The distillation fractions (bp 103-110° C. under 1 mbar) containing the expected product are combined together. 498.9 g of 3-fluoro-6-methoxyquinoline (76%) are thus obtained in the form of a white solid which melts at 51-53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07396934B2 |
|---|
| Source dataset | uspto-grants-2008_07 |
|---|
| ORD ID | ord-c0bac5c29e454fdeb06e1e34f414efed |
|---|
| Source note | uspto-grants-2008_07 |
|---|