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HRID 245052作成日:2026年10月26日

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

https://huagongshe.com/reaction/245052

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Potassium BromideHCID 253877—
反応物Sodium HypochloriteHCID 23665760—
反応物(1R,2R)-trans-N-Boc-2-AminocyclopentanolHCID 45091953—
触媒2,2,6,6-Tetramethyl-piperidine 1-oxideHCID 10125083—
溶媒Sodium ChlorideHCID 5234—
溶媒DichloromethaneHCID 6344—
生成物tert-butyl N-(2-oxocyclopentyl)carbamateHCID 35796276.3%

反応条件

温度5 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658693B2
出典データセットuspto-grants-2014_02
ORD IDord-168dca8190654a0589aeb29b2d568a89
出典メモuspto-grants-2014_02