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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583531Generated: October 30, 2026

Acetate → HCID 53838877, compound

https://huagongshe.com/reaction/1583531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantCarbon TetrachlorideHCID 5943—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantPotassium hydroxide methanolHCID 23689386—
ReactantHCID 70465999HCID 70465999—
SolventAcetoneHCID 180—
SolventO-XyleneHCID 7237—
SolventTetrahydrofuranHCID 8028—
SolventBenzene ethyl acetateHCID 21583983—
ProductHCID 53838877HCID 5383887721.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the acetate (14) (19 mg, 0.0396 mmol) in carbontetrachloride (2 ml) N-bromosuccinimide (10 mg, 0.0571 mmol) was added and this mixture was refluxed under argon atmosphere for 20 min. After cooling to 0° C., the resulting precipitate was filtered off. The filtrate was concentrated below 40° C. to leave the residue. This residue in xylene (2 ml) was added dropwise to a refluxing solution of S-collidine (0.5) and xylene (1.5 ml) and refluxing was continued for 20 min. The usual work-up (ethyl acetate for extraction) gave the crude diene. This diene in acetone (10 ml) was treated with a catalytic amount of TsOH at room temperature under argon atmosphere in the dark for 14 hr. The usual work-up (ethyl acetate for extraction) gave the crude 5,7-diene acetate. This acetate in THF (5 ml) was treated with 5% KOH-MeOH (1.0 ml) at room temperature under argon atmosphere in the dark for 30 min. The usual work-up (ethyl acetate for extraction) gave a crude product, which was submitted to preparative TLC (benzene-ethyl acetate 2:1, developed twice). The band of Rf value 0.47 was scraped off and eluted with ethyl acetate. Removal of the solvent provided the 5,7-diene (15) (3.75 mg, 21.7%). UV λmax mm: 294, 282, 272.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552698
Source datasetuspto-grants-1985_11
ORD IDord-fb5c4107d7e249a583794b1398f3d1e7
Source noteuspto-grants-1985_11