HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974828Generated: October 23, 2026
Bromine → 6-Bromo-3,4-dihydro-4,4,5,8-tetramethyl-2H-1-benzothiopyran
https://huagongshe.com/en/reaction/974828
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4,4,5,8-Tetramethylthiochroman | HCID 12993684 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-3,4-dihydro-4,4,5,8-tetramethyl-2H-1-benzothiopyran | HCID 12993685 | 87.1% |
Reaction Steps
100 ml of methylene chloride was added to 13.2 g (0.064 mol) of 4,4,5,8-tetramethylthiochroman, 10.2 g (0.064 mol) of bromine was dropwise added at room temperature, and then the mixture was allowed to react for 2 hours. After the completion of the reaction, 70 ml of a 2% sodium hydrogensulfite aqueous solution was added, excessive bromine was removed, and the reaction mixture was liquid-separated. An organic layer was washed with a saturated sodium hydrogencarbonate aqueous solution and with a saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate. The methylene chloride was distilled off under reduced pressure, and the resultant oily substance was purified by silica gel column chromatography to give 15.9 g (yield 87%) of 4,4,5,8-tetramethyl-6-bromothiochroman.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607898 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-fd493c7ac10046d5a2040544cffa57af |
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| Source note | uspto-grants-1997_03 |
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