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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668728Generated: November 3, 2026

Triethylamine → HCID 57825247, compound

https://huagongshe.com/reaction/1668728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantCyclohexane ethylacetateHCID 21867204—
ReactantHCID 67344941HCID 67344941—
SolventDichloromethaneHCID 6344—
ProductHCID 57825247HCID 57825247—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-[1-(4-Fluoro-3-bromo-phenyl)-vinyl]-phenol was produced from {4-[1-(3-bromo-4-fluoro-phenyl)-vinyl]-phenoxy}-tert-butyl-dimethyl-silane according to Building Block X & AA. To a solution of 4-[1-(4-fluoro-3-bromo-phenyl)-vinyl]-phenol (1.5 g, 4.88 mmol, 1.0 eq) in DCM (15 mL), triethylamine (2.0 mL, 14.65 mmol, 3.0 eq) was added and the reaction mixture cooled to 0° C. Then methanesulfonyl chloride (0.416 mL, 5.37 mmol, 1.1 eq) was added dropwise and the mixture was allowed to warm to room temperature and stirred 16 h. The reaction was examined by TLC (ethyl acetate/cyclohexane 20%) which showed complete conversion to the desired product. After night time water was added and organic and water phase were separated. Organic solution was dried over magnesium sulfate filtered and evaporated. The crude was purified by flash chromatography eluting with cyclohexane, then ethyl acetate/cyclohexane 20%. 1.4 g of clean product was obtained as colorless liquid (yield: 75%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989449B2
Source datasetuspto-grants-2011_08
ORD IDord-136db931c8744c018b79b8adf1f06c7e
Source noteuspto-grants-2011_08