돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245052생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/245052

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Potassium BromideHCID 253877—
반응물Sodium HypochloriteHCID 23665760—
반응물(1R,2R)-trans-N-Boc-2-AminocyclopentanolHCID 45091953—
촉매2,2,6,6-Tetramethyl-piperidine 1-oxideHCID 10125083—
용매Sodium ChlorideHCID 5234—
용매DichloromethaneHCID 6344—
생성물tert-butyl N-(2-oxocyclopentyl)carbamateHCID 35796276.3%

반응 조건

온도5 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658693B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-168dca8190654a0589aeb29b2d568a89
출처 메모uspto-grants-2014_02