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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant4,4,5,8-TetramethylthiochromanHCID 12993684—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
Product6-Bromo-3,4-dihydro-4,4,5,8-tetramethyl-2H-1-benzothiopyranHCID 1299368587.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607898
Source datasetuspto-grants-1997_03
ORD IDord-fd493c7ac10046d5a2040544cffa57af
Source noteuspto-grants-1997_03