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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602129생성일: 2026년 10월 23일

Potassium Bromide → Benzyl 3-formylpiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/602129

반응식

참여 물질

역할이름HCID투입량
반응물Potassium BromideHCID 253877—
반응물Sodium BicarbonateHCID 516892—
반응물Benzyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2776577—
반응물Sodium HypochloriteHCID 23665760—
촉매TempoHCID 2724126—
용매DichloromethaneHCID 6344—
생성물Benzyl 3-formylpiperidine-1-carboxylateHCID 989965390%

반응 단계

An aqueous solution (2 mL) of potassium bromide (983 mg, 8.26 mmol) was added to 1-benzyloxycarbonyl-3-piperidinyl methanol (2.00 g, 8.02 mmol) and 2,2,6,6-tetramethyl piperidine-N-oxyl (12.5 mg, 0.0802 mmol) in dichloromethane (20 mL). The mixture was stirred for 5 min while chilled in an ice bath. A 0.35 mol/L aqueous sodium hypochlorite solution (25.2 mL, 8.82 mmol) and sodium bicarbonate (1.96 g, 23.3 mmol) were added and the mixture was stirred for 10 min. Subsequently, the reaction mixture was extracted with ethyl acetate and the extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=10:1->2:1) gave 1.78 g (90%) of the desired compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902367B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-6e270006b9de40f4a66816fc7ecc256c
출처 메모uspto-grants-2011_03