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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398768Generated: October 31, 2026

Dibenzothiophene → 1-(Dibenzo[b,d]thiophen-2-yl)ethan-1-one

https://huagongshe.com/reaction/2398768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzothiopheneHCID 3023—
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
Product1-(Dibenzo[b,d]thiophen-2-yl)ethan-1-oneHCID 312027—

Reaction Steps

Dibenzothiophene (18.4g.) and anhydrous aluminium chloride (13.3g.) were mechanically stirred in carbon disulphide (100 ml.) while acetyl chloride (7.85g.) in carbon disulphide (20 ml.) was added dropwise over 0.5 hr. The temperature of the mixture rose to 30° C. After a total of 4 hr. stirring the mixture was poured on to ice and extracted with chloroform. The extract was washed with sodium bicarbonate solution, dried with magnesium sulphate, and evaporated. The residue was distilled under vacuum and a fraction, b.pt. 160°-180° C. at 0.6 mm. Hg, was extracted by boiling with ether, and the residue recrystallised twice from methanol to give colourless crystals of 2-acetyldibenzothiophene m.pt. 97°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025635
Source datasetuspto-grants-1977_05
ORD IDord-c046e91861f948f7a190bfa5eef1eaf6
Source noteuspto-grants-1977_05