HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 405781Erstellt: 25. Oktober 2026
Dimethyl Sulfoxide → 6-((benzyloxy)methyl)dihydro-2H-pyran-3(4H)-one
https://huagongshe.com/reaction/405781
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 6-(benzyloxymethyl)tetrahydro-2H-pyran-3-ol | HCID 58063706 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 6-((benzyloxy)methyl)dihydro-2H-pyran-3(4H)-one | HCID 58063632 | — |
Reaktionsschritte
DMSO (1.15 mL, 16.2 mmol) was added to a stirred solution of oxalyl chloride (1 mL, 10.8 mmol) in dichloromethane (60 mL) at −78° C. After 10 minutes, a dichloromethane solution of 6-(benzyloxymethyl)tetrahydro-2H-pyran-3-ol (14) (1.20 g, 5.40 mmol) was added. Stirring was continued for one hour then triethylamine (3.8 mL, 27 mmol) was added and slowly warmed to 0° C. The reaction was poured into saturated NH4Cl solution and the organic phase was washed with brine and dried (NaSO4). The residue was purified over silica gel using EtOAc and hexanes to give 6-(benzyloxymethyl)dihydro-2H-pyran-3(4H)-one (15).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754071B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-3663cbdaaeb047ac91dd5d57d64ae722 |
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| Quellennotiz | uspto-grants-2014_06 |
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