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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288355Generated: October 31, 2026

1-Chloro-4-acetoxynonane → 7-[N-(4(R)-hydroxy-2-nonynyl)acetamido]heptanoic acid

https://huagongshe.com/reaction/1288355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-acetoxynonaneHCID 13104716—
Reactant1-Chloro-4-acetoxy-5,5-dimethylnonaneHCID 20386107—
Reactantethyl 7-[N-(4-acetoxy-5,5-dimethylnonyl)acetamido]heptanoateHCID 21503963—
Product7-[N-(4(R)-hydroxy-2-nonynyl)acetamido]heptanoic acidHCID 22793820—

Reaction Steps

The synthesis of this compound is carried out as described in Example 2 except that, in Step B, the 1-chloro-4-acetoxynonane is replaced by an equimolar amount of 1-chloro-4-acetoxy-5,5-dimethylnonane (Example G, Step 3). The product in Step B is ethyl 7-[N-(4-acetoxy-5,5-dimethylnonyl)acetamido]heptanoate. The subsequent step yields 7-[N-(4-hydroxy-5,5-dimethylnonyl)acetamido]-heptanoic acid (C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987091
Source datasetuspto-grants-1976_10
ORD IDord-1d48e0ae950247b084e1a775ec8a1bb6
Source noteuspto-grants-1976_10