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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 7-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}-2-methylheptanoateHCID 20327677—
CatalystHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product7-[N-(4-hydroxynonyl)methanesulfonamido]-2-methylheptanoic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04033996
Source datasetuspto-grants-1977_07
ORD IDord-dc4df621e24e442bb7b744fbb8d979db
Source noteuspto-grants-1977_07