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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671787Generated: November 1, 2026

1,3-Propanedithiol → HCID 10104703, compound

https://huagongshe.com/reaction/1671787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanedithiolHCID 8013—
ReactantN-bromobutanimideHCID 67184—
Reactanto-FluorobenzaldehydeHCID 67970—
SolventDichloromethaneHCID 6344—
ProductHCID 10104703HCID 1010470378.2%

Reaction Steps

To a solution of 2-fluorobenzaldehyde (10.03 g, 80.8 mmol, 1.0 eq.) and NBS (2.16 g, 12.1 mmol, 0.2 eq.) in CH2Cl2 (400 mL) was added 1,3-propanedithiol (9.8 mL, 97.6 mmol, 1.2 eq.). After 0.75 h, the reaction mixture was concentrated in vacuo. The residue was diluted with CH2Cl2 and water, and the layers were separated. The organic layer was dried over Na2SO4, filtered, concentrated in vacuo, and triturated with hexanes to give 2-(2-fluorophenyl)-1,3-dithiane as a white solid (13.55 g, 78% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994337B2
Source datasetuspto-grants-2011_08
ORD IDord-35dfa3b325754d518589164e578e43c9
Source noteuspto-grants-2011_08