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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Propanedithiol | HCID 8013 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Dimethylamino)-1-(4-fluorophenyl)-2-methyl-3-phenylpropan-1-one | HCID 18755066 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1-[3-(Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-propan-1-one | HCID 54184036 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022906 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-e65a01732658481297562396df6567fe |
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| Source note | uspto-grants-2000_02 |
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