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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229166Generated: October 26, 2026

(4-Bromophenyl)(4-hydroxyphenyl)methanone → 4-[(4-Bromophenyl)(2,2,6,6-tetramethyltetrahydro-4H-pyran-4-ylidene)methyl]phenol

https://huagongshe.com/reaction/229166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Bromophenyl)(4-hydroxyphenyl)methanoneHCID 4570728—
Reactant2,2,6,6-Tetramethyloxan-4-oneHCID 11829691—
Reactant4-[(4-Bromophenyl)(tetrahydro-4H-pyran-4-ylidene)methyl]phenolHCID 68654197—
CatalystZincHCID 23994—
CatalystTitanium TetrachlorideHCID 24193—
Product4-[(4-Bromophenyl)(2,2,6,6-tetramethyltetrahydro-4H-pyran-4-ylidene)methyl]phenolHCID 6865432576%

Reaction Steps

Following the procedure described for compound 46, zinc powder (0.957 g, 14.6 mmole), TiCl4 (0.800 mL, 7.30 mmole), (4-bromophenyl)(4-hydroxyphenyl)methanone (2) (0.512 g, 1.85 mmole) and 2,2,6,6-tetramethyltetrahydro-4H-pyran-4-one (52) (0.851 mL, 5.45 mmole), afforded 0.564 g (76%) of 53 as a white foamy solid. 1H NMR (CDCl3): δ 7.41 (d, J=8.3 Hz, 2H), 7.02 (d, J=8.4 Hz, 2H), 7.01 (d, J=8.4 Hz, 2H), 6.76 (d, J=8.3 Hz, 2H), 4.99 (s, 1H), 2.24 (s, 2H), 2.20 (s, 2H), 1.22 (s, 6H), 1.21 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560589B2
Source datasetuspto-grants-2009_07
ORD IDord-3676bf1076144ab080b4fe3cc1bd7d5e
Source noteuspto-grants-2009_07