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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38995Erstellt: 24. Oktober 2026

Sodium Hydroxide → [(2S)-7-(Methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methanol

https://huagongshe.com/de/reaction/38995

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktL-ProlineHCID 145742—
EduktSodium methanesulfinateHCID 2733271—
Edukt(S)-(7-Bromo-2,3-dihydrobenzo[b][1,4]dioxin-2-yl)methanolHCID 23394142—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt[(2S)-7-(Methylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methanolHCID 66879136213,6%

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A mixture of [(2S)-7-bromo-2,3-dihydro-1,4-benzodioxin-2-yl]methanol (0.6 g, 2.3 mmol), sodium methanesulfinate (85%) (0.4 g, 3.4 mmol), CuI (0.043 g, 0.2 mmol), L-proline (0.052 g, 0.5 mmol) and NaOH (0.018 g, 0.5 mmol) in DMSO (3 ml) was heated under microwave radiation at 140° C. for 2 h 30 min in a nitrogen-flushed vial. The mixture was mixed with 2 other batches and water and EtOAc was added. The solution was extracted with EtOAc (3×50 ml). The combined organic phases were washed with LiCl (5%), HCl (1 N) and brine. The resulting solution was dried (Na2SO4) and evaporated to dryness. Purification on flash column chromatography (isooctane/EtOAc) gave the title compound (1.2 g). MS m/z (rel. intensity, 70 eV) 244 (M+, bp), 213 (39), 165 (26), 134 (22), 79 (23).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524766B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-03f4373c7a4a4431bff4e8401daf1f70
Quellennotizuspto-grants-2013_09