HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224866Generated: October 30, 2026
Methanol → 2-Chloro-5,6-dimethylnicotinaldehyde
https://huagongshe.com/reaction/224866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-Chloro-5,6-dimethylpyridine-3-carbonitrile | HCID 12891106 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-5,6-dimethylnicotinaldehyde | HCID 12783846 | 60.5% |
Reaction Steps
A mixture of 2-chloro-3-cyano-5,6-dimethylpyridine (21.5 g) semicarbazide hydrochloride (24.0 g), sodium acetate (42.3 g), water (225 ml) and methanol (475 ml) was hydrogenated at 344 kPa at 50° using Raney nickel catalyst (5 g). The mixture was added to water (750 ml) and filtered. The solid filtered off was suspended in water (130 ml) and concentrated hydrochloric acid (70 ml) was added and the mixture was heated at 100° for 1 hour, formalin (40% w/w, 120 ml) was added and the mixture was heated at 100° for a further 0.5 hour and allowed to cool. Sodium acetate (95 g) and water (250 ml) were added and the mixture was extracted with ether and the extracts were washed with 5% aqueous potassium carbonate and evaporated to give 2-chloro-5,6-dimethyl-3-pyridinecarboxaldehyde (13.24 g, 60%) m.p. 69°-70°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04234588 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-1782120f6fed4912a97a535f5967a625 |
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| Source note | uspto-grants-1980_11 |
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