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HRID 570128Erstellt: 24. Oktober 2026
Triethylamine → 2,2-Difluoropropane-1,3-diyl dimethanesulfonate
https://huagongshe.com/de/reaction/570128
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 2,2-Difluoropropane-1,3-diol | HCID 95744 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,2-Difluoropropane-1,3-diyl dimethanesulfonate | HCID 242871 | 84% |
Reaktionsschritte
To a solution of 5 g (44.6 mmol) 2,2-difluoropropane-1,3-diol (prepared as described in J. Med. Chem. 1994, 37, 1857-1864) in DCM (50 mL) was added triethylamine (18.6 mL, 133.83 mmol) and methane sulphonyl chloride (6.9 mL, 89.22 mmol) at 0° C. and stirred for 1 h at 0° C. Thereafter the reaction mixture was quenched with water and extracted with DCM. The organic layer was dried over anhydrous sodium sulphate and concentrated to afford 2,2-difluoropropane-1,3-diyl dimethanesulfonate (9 g, 84%) which was used immediately in the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09023844B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-6897520d27f9497e907addb4497dad07 |
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| Quellennotiz | uspto-grants-2015_05 |
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