HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376983Generated: October 26, 2026
1,3-Propanedithiol → 1-[4'-(3-Mercapto-propylthio)-biphenyl-4-yl]-2-methyl-2-morpholin-4-yl-propan-1-one
https://huagongshe.com/reaction/376983
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanedithiol | HCID 8013 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bisphenol A diglycidyl ether diacrylate | HCID 92212 | — |
| Reactant | 1-(4'-Bromo-biphenyl-4-yl)-2-methyl-2-morpholin-4-yl-propan-1-one | HCID 19360622 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1-[4'-(3-Mercapto-propylthio)-biphenyl-4-yl]-2-methyl-2-morpholin-4-yl-propan-1-one | HCID 19360597 | — |
Reaction Steps
3.5 g (9.0 mmol) of 1-(4'-Bromo-biphenyl-4-yl)-2-methyl-2-morpholin-4-yl-propan-1-one (prepared by the method described in EP-A-3002) and 5.4 ml (54 mmol) of 1,3-propanedithiol are dissolved in 50 ml of dimethylacetamide, and the solution is stirred at around 140° C. together with 2.5 g of potassium carbonate for 2.5 h. Then the solution is cooled to room temperature and poured into water. The crude product is extracted with methylene chloride, washed with saturated sodium chloride solution, dried over MgSO4, and concentrated. The residue is purified by column chromatography on silica gel with ethyl acetate-hexane (10:90) as an eluent. The structure is confirmed by the 1H-NMR spectrum (CDCl3): δ [ppm] 1.35 (s, 6H), 1.38 (t, 1H), 1.98 (tt, 2H), 2.61 (t, 4H), 2.69 (dt, 2H), 3.11 (t, 2H), 3.72 (t, 4H), 7.42 (d, 2H), 7.51 (d, 2H), 7.62 (d, 2H), 8.63 (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-44b9701d98794277954c24870002d79a |
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| Source note | uspto-grants-2000_02 |
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