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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716029Generated: November 1, 2026

Cyclohexanone → 4-[(4-Bromo-3-methylphenyl)(cyclohexylidene)methyl]phenol

https://huagongshe.com/reaction/1716029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
Reactant(4-Bromo-3-methylphenyl)(4-hydroxyphenyl)methanoneHCID 68654843—
CatalystZincHCID 23994—
CatalystTitanium TetrachlorideHCID 24193—
SolventTetrahydrofuranHCID 8028—
Product4-[(4-Bromo-3-methylphenyl)(cyclohexylidene)methyl]phenolHCID 6865452285%

Reaction Steps

Titanium tetrachloride (2.70 mL, 24.5 mmol) was added dropwise to a suspension of zinc powder (3.24 g, 49.5 mmol) in anhydrous THF (60 mL) at RT. After refluxing for 1 h, a mixture of 66 (1.78 g, 6.11 mmol) and cyclohexanone (1.80 g, 18.3 mmol) dissolved in THF (20 mL) was added dropwise. Refluxing was continued for 30 min. The reaction mixture was cooled to RT and filtered through Celite. Water (250 mL) was added and the mixture was extracted with Et2O (3×100 mL). The combined ethereal extracts were washed with water (200 mL), brine (200 mL), and dried over MgSO4. Concentration followed by flash chromatography (20:1 to 5:1 hexanes:EtOAc) afforded 1.85 g (85%) of 67 as an orange solid. 1H NMR (400 MHz, CDCl3): δ 1.58 (m, 6H), 2.20 (m, 4H), 2.32 (s, 3H), 5.95 (br s, 1H), 6.73 (d, J=8.4 Hz, 2H), 6.79 (dd, J=8.1 Hz, 2.0 Hz, 1H), 6.95 (m, 3H), 7.40 (d, J=8.1 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799828B2
Source datasetuspto-grants-2010_09
ORD IDord-82d2d9857e994d24b344b10cbbf5eab4
Source noteuspto-grants-2010_09