HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372534Generated: October 30, 2026
Acetic Anhydride → HCID 20327652, compound
https://huagongshe.com/reaction/372534
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 9885481 | HCID 9885481 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20327652 | HCID 20327652 | — |
Reaction Steps
A mixture of 7-[N-(4-hydroxynonyl)methanesulfonamido]heptanoic acid (10.9 g., 0.03 mole) (Example 1, Step B) and acetic anhydride (6.1 g., 0.06 mole) is heated at 60° C. for 18 hours. The mixture is cooled and 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 basic solution is separated and acidified with concentrated hydrochloric acid. The crude product 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. There is obtained 7-[N-(4-acetoxynonyl)methanesulfonamido]heptanoic acid as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04091107 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-87a23dd6e5744a24aa8abb12b3ffec74 |
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| Source note | uspto-grants-1978_05 |
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