HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960177Generated: October 30, 2026
Ethenone, dichloro- → HCID 13924057, compound
https://huagongshe.com/reaction/1960177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethenone, dichloro- | HCID 78338 | — |
| Reactant | 2(1H)-Pentalenone, 4-(5-ethoxyheptyl)hexahydro- | HCID 10400739 | — |
| Reactant | HCID 13924082 | HCID 13924082 | — |
| Reactant | HCID 131730366 | HCID 131730366 | — |
| Product | HCID 13924057 | HCID 13924057 | — |
| Product | HCID 13924060 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410314B1 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-f704d940ab8942d8bd3670057c9f1959 |
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| Source note | uspto-grants-2013_04 |
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