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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258609Generated: October 26, 2026

ethyl 4-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}butoxyacetate → 7-[N-(4(R)-hydroxy-2-nonynyl)methanesulfonamido]heptanoic acid

https://huagongshe.com/reaction/258609

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 4-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}butoxyacetateHCID 20327707—
ReactantEthyl 2-(4-bromobutoxy)acetateHCID 20436843—
ReactantEthyl 7-bromo-2-methylheptanoateHCID 22770549—
Product7-[N-(4(R)-hydroxy-2-nonynyl)methanesulfonamido]heptanoic acidHCID 22798404—

Reaction Steps

The synthesis of this compound is carried out as described in Example 8 except that, in Step A, the ethyl 7-bromo-2-methylheptanoate is replaced by an equimolar amount of ethyl 4-bromobutoxyacetate (Example M). The product of Step A is thus ethyl 4-{N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamido}butoxyacetate. The subsequent step yields 4-[N-(4-hydroxynonyl)methanesulfonamido]butoxyacetic acid (B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04033996
Source datasetuspto-grants-1977_07
ORD IDord-0a20112412f746a780939a517870c513
Source noteuspto-grants-1977_07