HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989390Generated: October 31, 2026
Nitric Acid → 4-(2-Chloroethoxy)-5-methoxy-2-nitrobenzaldehyde
https://huagongshe.com/reaction/989390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 4-(2-Chloroethoxy)-3-methoxybenzaldehyde | HCID 10775023 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(2-Chloroethoxy)-5-methoxy-2-nitrobenzaldehyde | HCID 21956382 | 40% |
Reaction Steps
Fuming nitric acid (10 mL) is added dropwise to a −40° C. suspension of 5.00 g (23.36 mmol) of 4-(2-chloroethoxy)-3-methoxybenzaldehyde (Milbank, J. B. J., et. al., J. Med. Chem., 42(4), 649-658, 1999) in 23 mL of 1,2-dichloroethane. The reaction mixture is slowly allowed to warm to −10° C. The mixture is poured onto 300 mL of ice water and then extracted with ethyl acetate. The organic layer is dried over magnesium sulfate, filtered and concentrated in vacuo. Diethyl ether is added to the residue and the pale yellow solid is collected by filtration to provide 2.43 g (40%) of 4-(2-chloroethoxy)-5-methoxy-2-nitrobenzaldehyde, mp 148-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06638929B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-072dc079392344c8bbaff9ac7698360b |
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| Source note | uspto-grants-2003_10 |
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