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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415432Generated: November 1, 2026

Thionyl Chloride → HCID 54316934, compound

https://huagongshe.com/reaction/1415432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-(2-oxocyclododecyl)propanoic acidHCID 2775083—
SolventBenzeneHCID 241—
ProductHCID 54316934HCID 54316934—

Reaction Steps

Ten parts of β-(2-oxocyclododecyl)propionic acid, 6 parts of thionyl chloride, and 35 parts of anhydrous benzene were placed into a reactor and allowed to stand at 0° C for 3 hours and further at room temperature overnight. Then, the excess amount of thionyl chloride and the benzene were distilled off under reduced pressure to give β-(2-oxocyclododecyl)propionic acid chloride. The acid chloride was dissolved in 25 parts of benzene. Into the resulting solution was added dropwise 35 parts of benzene solution containing 30 wt.% pyridine and the mixture was stirred for 6 hours. The produced crystals were filtered off. The filtrate was washed with dilute hydrochloric acid to remove excess pyridine, the organic layer was washed to remove the hydrochloric acid, and then dried with Glauber's salt. Thereafter the resulting solution was treated by the same method as in Example 1 to give 6.3 parts of 13-oxabicyclo(10.4.0)-hexadec-1(12)-en-14-one in 68.4% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005107
Source datasetuspto-grants-1977_01
ORD IDord-873106bb22714aaabe4e7099473b4f51
Source noteuspto-grants-1977_01