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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095457Generated: October 25, 2026

Hydrochloric Acid → 3,7-Dibromodibenzo(b,d)thiophene

https://huagongshe.com/reaction/2095457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant3,7-Dibromo-dibenzothiophene 5,5-dioxideHCID 4071898—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product3,7-Dibromodibenzo(b,d)thiopheneHCID 80375948.1%

Reaction Steps

Lithium aluminum hydride (4.1 g) is slowly introduced in small amounts over 50 minutes, in an ice bath, into a mixture of 3,7-dibromodibenzothiophene dioxide (20 g) and anhydrous ether (200 ml) in a 500-ml flask, and the mixture is heated to reflux and stirred for 2 hours. Water (200 ml) is added thereto to deactivate lithium aluminum hydride, and chloroform (200 ml) and concentrated hydrochloric acid (40 ml) are added to the mixture. The resulting mixture is thoroughly stirred, and the organic layer is separated. The aqueous layer is further extracted with chloroform (200 ml×2), and the extract is combined with the organic layer. The combined organic layer is washed with water (200 ml) and saturated brine (200 ml), and is dried over calcium chloride. The solvent is distilled off, and colorless crystals thus obtained are recrystallized from ethyl acetate+ethanol (16:3). Thus, 8.8 g of 3,7-dibromodibenzothiophene is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445900B2
Source datasetuspto-grants-2013_05
ORD IDord-6722264f6fb54c5586c7caf7d6811fc0
Source noteuspto-grants-2013_05