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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652608Generated: October 31, 2026

Benzyl Bromide → HCID 13558565, compound

https://huagongshe.com/reaction/652608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-dichloro-5-hydroxy-9,10-AnthracenedioneHCID 10891675—
SolventAcetoneHCID 180—
ProductHCID 13558565HCID 1355856587%

Reaction Steps

A mechanically stirred mixture of 177.2 g (0.605 mol) of 1,4-dichloro-5-hydroxy-9,10-anthracenedione (1, British Pat. No. 1,029,448), 83.5 g (0.605 mol) of powdered anhydrous potassium carbonate, 79 ml (0.675 mol) of benzyl bromide, and 1.7 l of dry acetone was heated at reflux for three days. The initial dark brown suspension changed to an olive green color signaling the end of the reaction. The mixture was filtered hot and the salts were washed with hot acetone. The cooled filtrate was concentrated to ~1/2 of its volume. The yellow precipitate was collected by filtration, washed with acetone and methanol, and dried at 200 mm/50° C./12 hr to leave 201.2 g (87%) of 2, mp 122°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04672129
Source datasetuspto-grants-1987_06
ORD IDord-9628d64a65d4453cb77984bb810a20de
Source noteuspto-grants-1987_06