HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484047Generated: October 30, 2026
2-Ethylbutyraldehyde → HCID 11789454, compound
https://huagongshe.com/reaction/484047
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Ethylbutyraldehyde | HCID 7359 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 11789454 | HCID 11789454 | — |
Reaction Steps
A reaction vessel was charged sequentially with Et3N (12.8 L), propionic anhydride (14.48 L), dimethylaminopyridine (94 gm) and 2-ethylbutyraldehyde (7.5 L). The mixture was stirred and heated under gentle reflux (120°-135° C.) for 5 hours in a nitrogen atmosphere. The reaction was then cooled to 70° C. and H2O (13.5 L) was added slowly. On complete addition, the mixture was heated at reflux for 45 minutes and then cooled to room temperature before hexane (7.5 L) was added. The aqueous layer was separated and re-extracted with hexane (5 L) and the combined organic layers were washed with saturated NaHCO3 (2×7.5 L) before being evaporated in vacuo at 40° C. The residue (10 Kg) so obtained was fractionally distilled (b.p. 75°-80° C., 30-40 mm Hg) to give the required product (7.712 Kg) as a mobile liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05229381 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-2b7107e4e3fa436e9c9f00f73c4b15a4 |
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| Source note | uspto-grants-1993_07 |
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