Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376959Generated: October 30, 2026

1,3-Propanedithiol → 1-[3-(Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-propan-1-one

https://huagongshe.com/reaction/376959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanedithiolHCID 8013—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Dimethylamino)-1-(4-fluorophenyl)-2-methyl-3-phenylpropan-1-oneHCID 18755066—
SolventDimethylacetamideHCID 31374—
Product1-[3-(Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-propan-1-oneHCID 54184036—

Reaction Conditions

Temperature50 °C

Reaction Steps

22.8 g (0.21 mol) of 1,3-propanedithiol is dissolved in 50 ml of dry dimethylacetamide, 4.8 g of potassium carbonate are added and the mixture is heated to about 50° C. 10.0 g of 1-(4-fluorophenyl) 2-dimethylamino-2-benzyl-propan-1-one in 50 ml of dry dimethylacetamide are added dropwise. The suspension is stirred at 50° C. for 12 h, the solid is filtered off. The excess 1,3-propandithiol and dimethylacetamide are distilled off. To the residue toulene is added and the resulting precipitate is filtered off. After the toluene is distilled off, the residue is purified by column chromatography on silica gel with ethyl acetate-hexane (1:9) as eluent. The structure is confirmed by the 1H-NMR-spectrum, measured in CDCl3. The signals (δ in ppm) are 1.16 (s,3H), 1.40 (t, 1H), 2.02 (m,2H), 2.34 (s,6H), 2.71 (q,2H), 2.96 (d, 1H), 3.14 (t,2H), 3.68 (d,1H), 6.88 (m,2H), 7.12 (m,3H), 7.29 (d,2H), 8.44 (d,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022906
Source datasetuspto-grants-2000_02
ORD IDord-e65a01732658481297562396df6567fe
Source noteuspto-grants-2000_02