HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-Bromo-6-chloro-2-fluorobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-4-chloro-2-fluorobenzene | HCID 137275 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromo-6-chloro-2-fluorobenzaldehyde | HCID 59299457 | 169% |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in THF (50 mL) was slowly added to LDA (0.125 mol) in THF (600 mL) at −50° C. After addition the solution was warmed to −20° C. and then cooled to −50° C. and a solution of DMF (14.6 g, 0.20 mol) in THF (50 mL) was slowly added and the reaction mixture was warmed to ambient temperature. The reaction was quenched with water (250 mL) and extracted with ethyl acetate (2×150 mL) and the combined organic phases were dried (sodium sulfate) and concentrated. The solid residue was recrystallized from hexane to give 3-bromo-6-chloro-2-fluorobenzaldehyde (40.0 g, 0.169 mol): mp 92-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07314849B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-ff5d842662a34076b06c7b657fe5fc44 |
| Source note | uspto-grants-2008_01 |