HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20354Erstellt: 25. Oktober 2026
Oxiranemethanol, 4-methylbenzenesulfonate, (S)- → Toluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl ester
https://huagongshe.com/reaction/20354
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxiranemethanol, 4-methylbenzenesulfonate, (S)- | HCID 153296 | — |
| Edukt | HCID 178418816 | HCID 178418816 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Toluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl ester | HCID 87498269 | 75,5% |
Reaktionsschritte
Add dropwise over 5 minutes isobutylmagnesium bromide (4.4 mL, 8.8 mmol, 2 M in diethyl ether) to a solution of lithium tetrachlorocuprate (4.4 mL, 0.44 mmol, 0.1 M in tetrahydrofuran) cooled to −35-40° C. Dissolve (2S)-(+)-glycidyl tosylate (1.674 g, 7.73 mmol) in tetrahydrofuran (8 mL), cool to −40° C. and cannulate into the stirring Grignard reaction flask. Quench with saturated aqueous ammonium chloride (25 mL), pour supernate into saturated aqueous ammonium chloride (25 mL) and water and shake well. Wash with saturated aqueous sodium chloride, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 10:90 to 25:75 ethyl acetate:hexanes) to give the desired compound (1.6711 g, 75%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745438B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-3e73c66220eb47a0913b0234fe1c8597 |
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| Quellennotiz | uspto-grants-2010_06 |
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