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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372530Generated: October 30, 2026

1-Chloro-4-acetoxynonane → 7-[N-(4-Hydroxy-(E)-2-nonenyl)methanesulfonamido]heptanoic Acid

https://huagongshe.com/reaction/372530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-acetoxynonaneHCID 13104716—
Reactantethyl 7-[N-(4-acetoxy-(E)-2-nonenyl)methanesulfonamido]heptanoic acidHCID 20327696—
Reactant1-Bromo-4-acetoxy-2-noneneHCID 54048569—
Product7-[N-(4-Hydroxy-(E)-2-nonenyl)methanesulfonamido]heptanoic AcidHCID 20327672—

Reaction Steps

The synthesis of this compound is carried out as described in Example 1 except that, in Step A, the 1-chloro-4-acetoxynonane is replaced by an equimolar amount of 1-bromo-4-acetoxy-2-nonene (Example H). The product of Step A is thus ethyl 7-[N-(4-acetoxy-(E)-2-nonenyl)methanesulfonamido]heptanoic acid (B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091107
Source datasetuspto-grants-1978_05
ORD IDord-fa4fea24dbd849a7aad7c2fc7356aab1
Source noteuspto-grants-1978_05