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HRID 245052Erstellt: 24. Oktober 2026

Potassium Carbonate → tert-butyl N-(2-oxocyclopentyl)carbamate

https://huagongshe.com/de/reaction/245052

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktPotassium BromideHCID 253877—
EduktSodium HypochloriteHCID 23665760—
Edukt(1R,2R)-trans-N-Boc-2-AminocyclopentanolHCID 45091953—
Katalysator2,2,6,6-Tetramethyl-piperidine 1-oxideHCID 10125083—
LösungsmittelSodium ChlorideHCID 5234—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-butyl N-(2-oxocyclopentyl)carbamateHCID 35796276,3%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

2,2,6,6-Tetramethylpiperidine-N-oxide (2.2 g, 14.2 mmol) and potassium bromide (8.5 g, 71 mmol) are added to a solution of racemic trans-tert-butyl N-[2-hydroxycyclopentyl]carbamate (75 g, 283 mmol) in dichloromethane (285 mL). The mixture is cooled to 5° C. with stirring. A freshly prepared ice cooled (5° C.) sodium hypochlorite aqueous solution (766 mL, 566 mmol, pH adjusted to 7.5-8 by addition of 10 g of solid potassium carbonate) is added with stirring to the reaction mixture while keeping the temperature below 5° C. The mixture is stirred at 5° C. for an additional 30 min. The reaction mixture is diluted with saturated aqueous sodium chloride solution (150 mL). The organic layer is separated and evaporated. The oily red residue is purified over a silica gel pad, eluting with EtOAc/hexanes (1/3) to obtain the title compound as a cream colored solid (43 g, 76%). 1H-NMR (300 MHz, DMSO-d6) δ 6.99 (d, 1H, NH), 3.76 (q, 1H), 1.63-2.31 (m, 6H), 1.37 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658693B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-168dca8190654a0589aeb29b2d568a89
Quellennotizuspto-grants-2014_02