HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982219Generated: October 25, 2026
Hydrochloric Acid → 4,5-Dihydroxy-2-nitrobenzaldehyde
https://huagongshe.com/reaction/1982219
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-Chloromethoxy-4-hydroxy-2-nitrobenzaldehyde | HCID 11424752 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4,5-Dihydroxy-2-nitrobenzaldehyde | HCID 3782344 | 68.1% |
Reaction Steps
To a stirred, cooled (0° C.) dispersion of 1.52 g (0.00658 mol) of 5-chloromethoxy-4-hydroxy-2-nitrobenzaldehyde (10), 1 g AlCl3, and 10 ml dry dichloroethane, 2.4 ml of dry pyridine are added. During addition, the reaction mixture is protected from atmospheric moisture, and the temperature is kept below 35° C. When addition is complete, the temperature is raised to 47° C., and maintained for 18 hours. 6N HCl is added, keeping the temperature at 30°-35° C., until the mixture is acidic to Congo Red indicator paper. The acidic solution is extracted with diethyl ether, and the combined ether extracts are dried over Na2SO4. After filtration, the ether is removed at reduced pressure, giving 0.82 g (68%) of (1): mp 201°-202°° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04595765 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-23064ba024c24eb897ac24e7430ddb49 |
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| Source note | uspto-grants-1986_06 |
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