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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447555Generated: October 31, 2026

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

https://huagongshe.com/reaction/1447555

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 (18.4 g.) and anhydrous aluminium chloride (13.3 g.) were mechanically stirred in carbon disulphide (100 ml.) while acetyl chloride (7.85 g.) 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 numberUS04177257
Source datasetuspto-grants-1979_12
ORD IDord-a91bd4f2913a4cb4aaf54c2128207ff5
Source noteuspto-grants-1979_12