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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388546Generated: November 2, 2026

Potassium Carbonate → 2-chloro-11H-dibenzo[b,f][1,4]oxathiepine

https://huagongshe.com/reaction/1388546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenol, o-mercapto-(6CI,7CI,8CI)HCID 70718—
Reactant2-(Bromomethyl)-4-chloro-1-iodobenzeneHCID 9862384—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
Product2-chloro-11H-dibenzo[b,f][1,4]oxathiepineHCID 1293096345.1%

Reaction Steps

A solution of 125.6 g of 5-chloro-2-iodobenzyl bromide in 500 ml of dimethylformamide is added to a mixture of 640 ml of dimethylformamide, 52.4 g of potassium carbonate and 47.8 g of 2-hydroxythiophenol (R. Leuckart, J.Prakt.Chem. /2/ 41, 192, 1890). Then, the mixture is stirred for 1 hour at room temperature, treated with 57 g. of potassium carbonate and 4.5 g of copper and is refluxed for 6 hours. Dimethylformamide is distilled off under reduced pressure, the residue diluted with water and shaken with benzene. After filtration, the benzene layer is separated, washed with water, dried with potassium carbonate and evaporated. By distillation of the residue there are obtained 42.5 g (45%) of 2-chloro-11H-dibenz(b.f)-1,4-oxathiepin with a b.p. of 148°-168° C./85 Pa and m.p. of 66.76° C. The pure product is obtained by crystallization from methanol and melts at 78°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431808
Source datasetuspto-grants-1984_02
ORD IDord-af8a867f91d0437c9d3c138093d805b0
Source noteuspto-grants-1984_02