HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29500Generated: October 26, 2026
5-Chloro-2-nitrobenzaldehyde → (5-Chloro-2-nitro-phenyl)-(6-chloro-pyridin-3-yl)-methanol
https://huagongshe.com/reaction/29500
Participants
| Role | Name | HCID | Charge |
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| 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 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 |
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| Patent number | US07420055B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-63a7bf13d186452bada32640db498840 |
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| Source note | uspto-grants-2008_09 |
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