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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 879030Erstellt: 24. Oktober 2026

Dichloromethane → Benzyl hydroxycarbamate

https://huagongshe.com/de/reaction/879030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktBenzyl chloroformateHCID 10387—
EduktHydroxyamine hydrochlorideHCID 443297—
EduktSodium BicarbonateHCID 516892—
LösungsmittelWaterHCID 962—
ProduktBenzyl hydroxycarbamateHCID 1890770%
ProduktN,O-bis(benzyloxycarbonyl)hydroxylamineHCID 1182273713%

Reaktionsbedingungen

Temperatur2 °C

Reaktionsschritte

Hydroxylamine hydrochloride (8.31 g, 120 mmol) is dissolved in water (200 mL) followed by the introduction of sodium bicarbonate (17.7 g, 211 mmol). Then CH2Cl2 (200 mL) is added to the solution and resulting the mixture is cooled in an ice bath to 0-4° C. Benzyl chloroformate (16.7 mL, 117 mmol) is added with vigorous stirring while maintaining the temperature below 4° C. After addition is complete the reaction mixture is left to stir for 2 h. The biphasic reaction mixture is transferred into a separating funnel and CH2Cl2 is added until the organic phase clarified. The aqueous phase is extracted with CH2Cl2 (3×100 mL) and then washed with brine, dried over MgSO4 and concentrated to give a colourless solid. Flash column chromatography (silica gel, CH2Cl2 then ethyl acetate/petroleum spirits 3:7 then 1:0) affords 13.7 g (70%) of 51 as a colourless solid along with 4.60 g (13%) of 52 as a colourless oil. Spectroscopic data are identical to those reported above.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987504B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-815dc066c4824d4dbf0f0e9c06d1b560
Quellennotizuspto-grants-2015_03