HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6390Generated: October 26, 2026
1,3-Dithiane → 2-(3-Fluorophenyl)methyl-1,3-dithiane
https://huagongshe.com/reaction/6390
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dithiane | HCID 10451 | — |
| Reactant | 3-Fluorobenzyl bromide | HCID 68007 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(3-Fluorophenyl)methyl-1,3-dithiane | HCID 19793236 | 66.7% |
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 DCl--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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05248677 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-3d8b557851dd4629afee23bc916f9121 |
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| Source note | uspto-grants-1993_09 |
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