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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2376856Erstellt: 26. Oktober 2026

Triethylamine → Tert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylate

https://huagongshe.com/reaction/2376856

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium ThiosulfateHCID 24477—
Eduktm-Chloroperbenzoic acidHCID 70297—
EduktThiomorpholine, N-BOC protectedHCID 21949316—
Edukttert-Butoxycarbonyl dicarbonateHCID 86600350—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 1,1-dioxo-1lambda6-thiomorpholine-4-carboxylateHCID 2194926091,6%

Reaktionsschritte

tert-Butyl thiomorpholine-4-carboxylate (1.91 g, 9.42 mmol) was dissolved in dichloromethane (50 ml); m-chloroperbenzoic acid (5.0 g, 19 mmol) was gradually added while cooled with ice bath, stirred, and under nitrogen atmosphere; and the reaction mixture was stirred at room temperature for 12 hours. After addition of a saturated aqueous solution of sodium thiosulfate, the reaction mixture was kept stirred for a while; and this was subjected to extraction with ethyl acetate, washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Triethylamine (8.1 ml, 58 mmol) were added to the obtained crystals; and the reaction mixture was stirred at room temperature. tert-Butoxycarbonyl dicarbonate (13.3 ml, 58 mmol) was added thereto; and the reaction mixture was stirred at room temperature for 10 hours. The reaction mixture was concentrated under reduced pressure; and the obtained crystals were suspended with a solvent mixture of diethyl ether:ethanol=10:1, filtered off, washed with diethyl ether and dried under aeration to yield the title compound as colorless crystals (2.03 g, 8.63 mmol, 91.6%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07468380B2
Quelldatensatzuspto-grants-2008_12
ORD IDord-ca9ed8b2450f46f89d37934466d5ddf2
Quellennotizuspto-grants-2008_12