HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729931Generated: October 25, 2026
Acetic Anhydride → 7-{[4-(Acetyloxy)nonyl](carbamoyl)amino}heptanoic acid
https://huagongshe.com/reaction/1729931
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-[Carbamoyl(4-hydroxynonyl)amino]heptanoic acid | HCID 21501441 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 7-{[4-(Acetyloxy)nonyl](carbamoyl)amino}heptanoic acid | HCID 53945703 | — |
Reaction Steps
A mixture of 7-[1-(4hydroxynonyl)ureido]heptanoic acid (9.9 g., 0.03 mole) (Example 1, Step C) and acetic anhydride (6.1 g., 0.06 mole) is heated at 60° C. for 18 hours. The mixture is cooled and taken up in 80 ml. of ethyl ether. The solution is extracted with an ice-cold solution of 8 g. of sodium hydroxide in 150 ml. of water. The basis solution is separated and acidified with concentrated hydrochloric acid. The oil that separates is extracted into ether, washed with water and dried over sodium sulfate. The ether is evaporated and the residual oil is purified by chromatography on silica gel using 2% methanol in chloroform as the eluting solvent. Thus there is obtained 7-[1-(4-acetoxynonyl)ureido] heptanoic acid as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03989749 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-537c0d46c6654f0a888984f8e49d2622 |
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| Source note | uspto-grants-1976_11 |
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