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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288345Generated: November 2, 2026

Ethyl 7-bromoheptanoate → Ethyl 7-{acetyl[4-(acetyloxy)nonyl]amino}heptanoate

https://huagongshe.com/reaction/1288345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-bromoheptanoateHCID 122490—
Reactant1-Chloro-4-acetoxynonaneHCID 13104716—
ReactantHCID 21503952HCID 21503952—
ReactantEthyl 7-acetamidoheptanoateHCID 21503972—
ProductEthyl 7-{acetyl[4-(acetyloxy)nonyl]amino}heptanoateHCID 21503950—

Reaction Steps

The preparation of this compound is accomplished by essentially the same method as described in Example 1, Step A, except that the N-[4-(2-tetrahydropyranyloxy)nonyl]-acetamide of Example 1, Step A is replaced by an equimolar quantity of ethyl 7-acetamidoheptanoate and the ethyl 7-bromoheptanoate is replaced by an equimolar quantity of 1-chloro-4-acetoxynonane (Example A, Step 4). Purification of the product by column chromatography on silica gel gives ethyl 7-[N-(4-acetoxynonyl)acetamido]heptanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987091
Source datasetuspto-grants-1976_10
ORD IDord-ed8f2477a0d2458e8571e85f5f202046
Source noteuspto-grants-1976_10