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HRID 2210275Erstellt: 27. Oktober 2026
Bromine → 2-Bromo-5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno [3,2-b]pyran
https://huagongshe.com/reaction/2210275
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Bromine | HCID 24408 | — |
| Edukt | 5,6-Dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno[3,2-b]pyran | HCID 9903464 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Bromo-5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno [3,2-b]pyran | HCID 14986492 | — |
Reaktionsschritte
A solution of bromine (0.20 mL, 3.92 mmol) in dichloromethane (5 mL) was slowly added to a solution of 5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno[3,2-b]pyran (1.0 g, 3.74 mmol) at -5° C. The resultant mixture was stirred at rt for 2 h. The resulting precipitate was collected by filtration and purified by medium pressure chromatography using 5% methanol in dichloromethane as the eluant to give the product as a colorless solid, 0.28 g (22%): mp 162°-165° C.; IR(KBr): 3287, 1666 and 1570 cm-1 ; MS: m/z 346 (MH+); 1H NMR (CDCl3): δ1.30 (s, 3H), 1.47 (s, 3H), 2.06 (m, 2H), 7.50 (m, 2H), 3.23 (bs, 1H, exchanges with D2O), 3.34 (m, 2H), 3.76 (d, J=9.1 Hz, 1H) 5.16 (d, J=9.1 Hz, 1H) and 6.56 (s, 1H). Anal. Calcd. for C13H16BrNO3S: C, 45.10; H, 4.66; N, 4.05.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05457212 |
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| Quelldatensatz | uspto-grants-1995_10 |
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| ORD ID | ord-2d3b6922caec42cb9efe709a3b84e397 |
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| Quellennotiz | uspto-grants-1995_10 |
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