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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31362Erstellt: 23. Oktober 2026

Formaldehyde → HCID 135427951, Verbindung

https://huagongshe.com/de/reaction/31362

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktSodium HydroxideHCID 14798—
EduktBenzyl (S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamateHCID 135487328—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 135427951HCID 135427951—

Reaktionsschritte

A solution of benzyl [(1S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethyl]carbamate (30.83 g, 0.0949 mol) in THF (400 ml) was treated with aqueous concentrated formaldehyde (37%, 12 M. 0.285 mol, 24 mL) and cooled in an ice bath. To the mixture was slowly added aqueous 1 N sodium hydroxide (0.02 mol, 20 mL) and the reaction was allowed to warm to room temperature while stirring overnight. The reaction was quenched with aqueous saturated sodium bicarbonate (250 mL) and then neutralized to pH 7 with aqueous 2 N hydrochloric acid. The mixture was extracted with ethyl acetate (200 mL×3), the combined organic layers were dried over magnesium sulfate and filtered and evaporated to give crude tan solid, 28.38 g, which was a mixture of desired product and dimerized byproduct by LC/MS 356 m/z and 663 m/z. This residue was purified by chromatography (silica gel, hexane/ethyl acetate 1:1) to give the title compound, (18.44 g, 56%) as a yellow foamy solid, which was not pure by LS/MS 354 m/z with minor 663 m/z.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425572B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-bfb01c5aa2d84f0398523e4456f98058
Quellennotizuspto-grants-2008_09