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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3,7-Dibromo-dibenzothiophene 5,5-dioxide | HCID 4071898 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3,7-Dibromodibenzo(b,d)thiophene | HCID 803759 | 48.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445900B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-6722264f6fb54c5586c7caf7d6811fc0 |
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| Source note | uspto-grants-2013_05 |
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