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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333206Generated: October 29, 2026

ST4026352 → Benzene-1,3-diylbis[(4-hydroxyphenyl)methanone]

https://huagongshe.com/reaction/333206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantST4026352HCID 344097—
ReactantTrifluoroborane-methyl sulfideHCID 11137191—
SolventDichloromethaneHCID 6344—
ProductBenzene-1,3-diylbis[(4-hydroxyphenyl)methanone]HCID 22842038%

Reaction Steps

To a well-stirred solution of 1,3-bis-(4-methoxybenzoyl)benzene 14 (1.80 g, 5.2 mmol) in dichloromethane (85 mL) was added boron trifluoride dimethyl sulfide complex (BF3.SMe2, 15 mL). The mixture was stirred for 27 h. After the reaction was quenched by water, the mixture was extracted with ethyl acetate (3×80 mL). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated under vacuum. The resulting solid was further purified using flash chromatography (silica gel, hexanes:ethyl acetate, 50:50) to afford the pure 1,3-bis-(4-hydroxybenzoyl)benzene 20 (0.62 g, 1.95 mmol) as a white solid in a 38% yield; 1H NMR (500 MHz, Acetone-d6): δ 9.28 (s, OH), 8.04 (td, J=1.7 Hz, 1.3 Hz, 1H, ArH), 7.98 (dd, J=7.7 Hz, 1.75 Hz, 2H, ArH), 7.80 (ddd, J=9.5 Hz, 4.8 Hz, 2.75 Hz, 4H, ArH), 7.73 (td, J=7.9 Hz, 0.45 Hz, 1H, ArH), 7.00 (ddd, J=9.5 Hz, 4.8 Hz, 2.75 Hz, 4H, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877967B2
Source datasetuspto-grants-2014_11
ORD IDord-ce94d7cd33b94bbe9868141411e52270
Source noteuspto-grants-2014_11