HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258606Generated: October 29, 2026
Ethanol → 7-[N-(4-hydroxynonyl)methanesulfonamido]-2-methylheptanoic acid
https://huagongshe.com/reaction/258606
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 7-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}-2-methylheptanoate | HCID 20327677 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-[N-(4-hydroxynonyl)methanesulfonamido]-2-methylheptanoic acid | HCID 20327658 | — |
Reaction Steps
A soluton is prepared from ethyl 7-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}-2-methylheptanoate (4.9 g., 0.01 mole), ethanol (50 ml.), and 4 drops of hydrochloric acid (conc.), and kept at ambient temperature for 4.5 hours. Then to the reaction is added a solution of sodium hydroxide (0.72 g., 0.018 mole) in water (10 ml.) and the reaction is kept at ambient temperature for an additional 20 hours. Most of the ethanol is removed in vacuo and the residue dissolved in water (100 ml.). The solution is extracted once with ether (75 ml.). then acidified with hydrochloric acid (dil.). The oil that separates is extracted into ether, the ether is washed with brine, dried over sodium sulfate, then removed under vacuum to give 7-[N-(4-hydroxynonyl)methanesulfonamido]-2-methylheptanoic acid as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04033996 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-dc4df621e24e442bb7b744fbb8d979db |
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| Source note | uspto-grants-1977_07 |
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