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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748972Generated: October 29, 2026

Toluene → HCID 68516997, compound

https://huagongshe.com/reaction/748972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosphorus tribromideHCID 24614—
Reactant3,4-Dihydro-6-methoxy-2-[4-(methylsulfonyl)phenyl]-1(2H)-naphthalenoneHCID 68518784—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68516997HCID 6851699774%

Reaction Steps

Add 2-(4-methanesulfonyl-phenyl)-6-methoxy-3,4-dihydro-2H-naphthalen-1-one (1.0 eq.), hyflo (20 wt %), and toluene (7.5 vols) to a three neck flask with a reflux condenser and nitrogen vent purge. While stirring at room temperature, add PBr3 (1.75 eq.) in one portion. Heat the reaction to reflux (˜110° C.) overnight allowing it to vent through a caustic scrubber. After refluxing for 15 hours, cool the yellow solution to 45° C. and slowly add THF (20 vols). Stir this mixture for 30 minutes at 45° and filter it, while warm, over a pad of Hyflo. Wash the pad with 45° C. THF (2×2 vols). Concentrate the filtrate at reduced pressure to remove all of the THF. Carefully add water (7.5 vols) to the remaining mixture keeping the temperature below 40° C. Cool the slurry to room temperature and stir it for 2 to 3 hours. Filter the slurry over a polypropylene pad and wash it with water (2×2 vols). Dry the resulting filter cake in a vacuum oven overnight at 50° C. to provide the title compound (74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399867B2
Source datasetuspto-grants-2008_07
ORD IDord-68830429961748b881a737b57aba3cab
Source noteuspto-grants-2008_07