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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452954Generated: November 3, 2026

1,3-Propanedithiol → HCID 10104703, compound

https://huagongshe.com/reaction/1452954

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 numberUS07473784B2
Source datasetuspto-grants-2009_01
ORD IDord-73c51fcdd265420f8035d2e36d5a4ded
Source noteuspto-grants-2009_01