HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451606Generated: October 30, 2026
1-Dodecanethiol → 1-Propanol, 3-(dodecylthio)-
https://huagongshe.com/reaction/1451606
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Dodecanethiol | HCID 8195 | — |
| Reactant | 3-Bromo-1-propanol | HCID 12308 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Propanol, 3-(dodecylthio)- | HCID 4172204 | 94.3% |
Reaction Steps
Dodecylthiol (5 g) was dissolved in 50 ml of dry N,N-dimethylformamide and 1 g of 60% sodium hydride was added thereto under ice-cooling. The mixture was stirred at room temperature for 1 hour. Further, a solution of 3.45 g of 3-bromopropanol in 10 ml of dry N,N-dimethylformamide was dropwise added thereto under ice-cooling and the mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into ice, extracted with ether and washed with 1N hydrochloric acid, a saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous sodium chloride solution. The ether layer was dehydrated and concentrated. The resultant mixture was purified by silica gel column chromatography using hexane-ethyl acetate (10:1→3:1) as an eluent to give 6.071 g of 3-dodecylthiopropanol as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604229 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-b29a7b42faee4a729ce1a21418a27947 |
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| Source note | uspto-grants-1997_02 |
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