HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358479Generated: October 30, 2026
Hydrochloric Acid → HCID 13373522, compound
https://huagongshe.com/reaction/358479
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Pyridinebutanoic acid, ethyl ester | HCID 11679975 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13373522 | HCID 13373522 | — |
Reaction Steps
A suspension of 2.53 g. of sodium hydride in 35 ml. of anhydrous dimethyl formamide was prepared. The suspension was cooled to about 0° C. with stirring. Next, a mixture of 9.56 g. of ethyl formate and 19 g. of ethyl 4-(3-pyridyl)butyrate were added. The consequent reaction mixture was stirred at about 0° C. for 1 additional hour and then at room temperature for about 3 days. The reaction mixture was acidified with 2N aqueous hydrochloric acid and the acidic aqueous solution evaporated to a very small volume in vacuo. The acidity of the solution was adjusted to pH=6 by the addition of solid potassium carbonate. The neutral aqueous layer was then extracted with ether. The ether layer was separated and dried. Evaporation of the ether yielded 16.4 g. of ethyl 2-formyl-4-(3-pyridyl)butyrate (formed in the above reaction) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04468399 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-5f89918373ff4aaf9f5f5c61206f441e |
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| Source note | uspto-grants-1984_08 |
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