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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646584Generated: October 27, 2026

1,3-Dithiane → 2-(3-Fluorophenyl)methyl-1,3-dithiane

https://huagongshe.com/reaction/1646584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DithianeHCID 10451—
Reactant3-Fluorobenzyl bromideHCID 68007—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-(3-Fluorophenyl)methyl-1,3-dithianeHCID 1979323666.7%

Reaction Conditions

Temperature-23 °C

Reaction Steps

1,3-Dithiane (12 g, 0.1 mol) was dissolved in 150 mL of anhydrous THF under a nitrogen atmosphere. The resultant solution was cooled to -78° C. and n-butyllithium (44 mL of a 2.5M solution of in hexane, 0.11 mol) was added. The reaction mixture was warmed to -23° C. and then stirred at -23° C. for 0.5 h. The reaction mixture was recooled to -78° C. and 25 g (0.135 mol) of 3-fluorobenzyl bromide was added over a 15 minute period. The reaction mixture was stirred for 3 h at ambient temperature and then diluted with methylene chloride, washed with aqueous ammonium chloride solution and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was distilled to afford 15.2 g (66.7% yield) of the title compound, b.p. 135°-140° C. (0.5 mm Hg); MS DCI-NH3M/Z: 229 (M+H)+ ; 1H NMR (CDCl3) δ1.77-1.95 (1H, m), 2.05-2.18 (1H, m), 2.8-2.9 (4H, m), 3.02 (2H, d, J=7.5 Hz), 4.23 (1H, t, J=7.5 Hz), 6.9-7.1 (3H, m), 7.23-7.33 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180733
Source datasetuspto-grants-1993_01
ORD IDord-f202a4206cc34fae9f58796f2eb83806
Source noteuspto-grants-1993_01