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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421205Generated: November 3, 2026

Tetrahydrothiophene → 2-Bromo-1-(phenanthren-2-yl)ethan-1-one

https://huagongshe.com/reaction/1421205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrothiopheneHCID 1127—
ReactantBromineHCID 24408—
ReactantMethyl 2-phenanthryl ketoneHCID 80060—
ReactantSulfoniumHCID 3015009—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-(phenanthren-2-yl)ethan-1-oneHCID 18780406—

Reaction Steps

Preparation of a sulfonium salt according to Formula 3 wherein X- is CF3SO3- and R1, R2, and S combined are tetrahydrothiophene is as follows. To a stirred solution of 5 grams (22.6 mM) of 2-acetylphenanthrene in a mixture of 30 ml of methylene chloride and 30 ml of diethyl ether cooled in an ice/acetone bath was added 3.5 grains (22 mM) of bromine dropwise over 15 minutes. The red bromine color was immediately discharged upon addition to the stirred solution. The cooling bath was removed and the stirred mixture warmed to room temperature over 30 minutes, then the mixture was stirred at room temperature for 2 hours. The reaction mixture was stripped of solvent on a rotary evaporator, then was suspended in 50 ml diethyl ether and evaporated to dryness. This process was repeated twice more to remove the byproduct hydrogen bromide from the solid product. The residual solid was triturated with 15 ml cold diethyl ether, filtered, and dried in a vacuum oven to yield 4.35 grams of 2-(bromoacetyl)-phenanthrene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06074800
Source datasetuspto-grants-2000_06
ORD IDord-fb7ad6239cee418ab2a2dfc7c9484093
Source noteuspto-grants-2000_06