HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1737450Erstellt: 26. Oktober 2026
N-Methylphenylethanolamine → HCID 21842621, Verbindung
https://huagongshe.com/reaction/1737450
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-Methylphenylethanolamine | HCID 913 | — |
| Edukt | Benzenesulfonyl chloride | HCID 7369 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 21842621 | HCID 21842621 | — |
Reaktionsschritte
A solution of α-(methylaminomethyl)benzyl alcohol (1.00 g, 6.61 mmol) in 15 mL of THF was cooled in an ice bath. Benzenesulfonyl chloride (0.886 mL, 1.23 g, 6.94 mmol) and N,N-diisopropylethylamine (2.3 mL, 1.7 g, 13 mmol) were added and mixture was allowed to warm to room temperature. After 30 min, the solvent was evaporated and the residue was partitioned between 50 mL of ethyl acetate and 40 mL of saturated aqueous sodium bicarbonate. The aqueous layer was extracted with 2×50 mL of ethyl acetate. The combined organic layers were washed with 50 mL of brine, dried over sodium sulfate, and evaporated. Purification by flash column chromatography on silica gel, eluting with 20-50% ethyl acetate in hexane, gave the title compound in quantitative yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05962462 |
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| Quelldatensatz | uspto-grants-1999_10 |
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| ORD ID | ord-ba598985bff041bf90162b74bd66b628 |
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| Quellennotiz | uspto-grants-1999_10 |
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