HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-nitrobenzaldehyde → (5-Chloro-2-nitro-phenyl)-(6-chloro-pyridin-3-yl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-nitrobenzaldehyde | HCID 81123 | — |
| Reactant | 2-Chloro-5-iodopyridine | HCID 4397176 | — |
| Reactant | HCID 178420663 | HCID 178420663 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Chloro-2-nitro-phenyl)-(6-chloro-pyridin-3-yl)-methanol | HCID 22327314 | — |
Reaction Conditions
| Temperature | -45 °C |
|---|
Reaction Steps
A solution of 1.0 g 2-chloro-5-iodopyridine (4.1 mmol, 1.0 eq.) in 10 mL anhyd. THF was stirred at −40° C. to −50° C. After five minutes, 2.2 mL of 2.1 M iPrMgBr/THF (4.6 mmol, 1.1 eq.) were added drop wise over 1 minute and the reaction mixture is maintained at −40 to −50° C. for 30 minutes. 1.3 g 2-nitro-5-chlorobenzaldehyde (7.0 mmol, 1.7 eq.) was then added and the reaction was maintained at −50° C. After 1 hour, the reaction was allowed to warm to −10° C., and quenched with 50 mL saturated brine after a further fifteen minutes. The crude product was extracted with EtOAc, dried on Na2SO4 and concentrated by rotary evaporation to yield desired product. MS: (M+H)/z=298.9
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08211896B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-be2efee133084b8593abea6ab07baf03 |
| Source note | uspto-grants-2012_07 |