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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960177Generated: October 30, 2026

Ethenone, dichloro- → HCID 13924057, compound

https://huagongshe.com/reaction/1960177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthenone, dichloro-HCID 78338—
Reactant2(1H)-Pentalenone, 4-(5-ethoxyheptyl)hexahydro-HCID 10400739—
ReactantHCID 13924082HCID 13924082—
ReactantHCID 131730366HCID 131730366—
ProductHCID 13924057HCID 13924057—
ProductHCID 13924060HCID 13924060—

Reaction Steps

Disclosed is a method of synthesizing a compound, such as 6-(5-ethoxyhept-1-yl)bicyclo[3.3.0]octan-3-one or methoxyheptyl bicyclooctanone, from 3-(5-ethoxyhept-1-yl)cyclopentene or other starting material. Such a method comprises reacting 3-(5-ethoxyhept-1-yl)cyclopentene with dichloroketene to form a first mixture comprising 7,7-dichloro-4-(5-ethoxyhept-1-yl)bicyclo[3.2.0]heptan-6-one and 6,6-dichloro-4-(5-ethoxyhept-1-yl)bicyclo[3.2.0]-heptan-7-one. The first mixture is reacted with acetic acid and zinc to form a second mixture comprising 4-(5-ethoxyhept-1-yl)bicyclo[3.2.0]heptan-6-one and 4-(5-ethoxyhept-1-yl)bicyclo-[3.2.0]heptan-7-one. The second mixture is reacted with trimethylsulfonium iodide to form a third mixture comprising 2-(5-ethoxyhept-1-yl)spiro[bicyclo[3.2.0]heptane-6,2′-oxirane]. The third mixture is reacted with lithium iodide to form 6-(5-ethoxyhept-1-yl)bicyclo[3.3.0]octan-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410314B1
Source datasetuspto-grants-2013_04
ORD IDord-f704d940ab8942d8bd3670057c9f1959
Source noteuspto-grants-2013_04