HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576663Generated: November 1, 2026
Hydrogen Bromide → HCID 67121893, compound
https://huagongshe.com/reaction/576663
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2',6'-Dimethyl-4'-(3-(methylsulfonyl)propoxy)(1,1'-biphenyl)-3-methanol | HCID 59342556 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67121893 | HCID 67121893 | — |
Reaction Steps
Concentrated sulfuric acid (1.4 g) was added dropwise to 48% hydrobromic acid (15 ml) at room temperature and [2′,6′-dimethyl-4′-[3-(methylsulfonyl)propoxy]-[1,1′-biphenyl]-3-yl]methanol (25 g) synthesized in accordance with the method described in [WO 2008/001931 pamphlet] was divided into five portions and added to the mixture. The reaction mixture was stirred at 60° C. for 2.5 hours and 48% hydrobromic acid (3.3 ml) was added to the mixture. The mixture was further stirred for 1 hour at the same temperature. After the reaction mixture was allowed to cool, water was added to the reaction mixture. The mixture was extracted with ethyl acetate. The obtained organic phase was washed with water, then washed with brine, and dried over anhydrous sodium sulfate. From the organic phase, the solvent was removed by evaporation under reduced pressure to give the title compound (27 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040525B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-dcf07838aa9248d3ba9bcdd09a8d285c |
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| Source note | uspto-grants-2015_05 |
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