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
Participants
| Role | Name | HCID | Charge |
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| Reactant | ST4026352 | HCID 344097 | — |
| Reactant | Trifluoroborane-methyl sulfide | HCID 11137191 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzene-1,3-diylbis[(4-hydroxyphenyl)methanone] | HCID 228420 | 38% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877967B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ce94d7cd33b94bbe9868141411e52270 |
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| Source note | uspto-grants-2014_11 |
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