HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 6-Chloro-2,4-difluoro-3-trimethylsilylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | (4-Chloro-2,6-difluorophenyl)trimethylsilane | HCID 18935733 | — |
| Reactant | Lithium tetramethylpiperidine | HCID 66701855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Chloro-2,4-difluoro-3-trimethylsilylbenzaldehyde | HCID 86613841 | 82.4% |
Reaction Steps
A solution of 1-chloro-3,5-difluoro-4-trimethylsilylbenzene (1.5 g, 6.8 mmol) in THF (10 mL) was added to a solution of lithium tetramethylpiperdine (14 mmol) in THF (15 mL) at −75° C. The solution was stirred for 2 hours then DMF (1.5 g, 20 mmol) was added and the solution allowed to warm to ambient temperature. The reaction was quenched with a saturated solution of ammonium chloride (25 mL) and extracted with ethyl ether (2×25 mL) and the combined extracts dried (sodium sulfate) and concentrated. The residue was purified by chromatography (hexanes) to give 6-chloro-2,4-difluoro-3-trimethylsilylbenzaldehyde (1.4 g, 5.6 mmol): LC/MS (m/z=248).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07314849B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-fef4a84f985b4d1c888cb07e736f6b4d |
| Source note | uspto-grants-2008_01 |