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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74994생성일: 2026년 10월 25일

Iodine → 4-Iodo-1-methyl-6-azabicyclo[3.2.1]octan-7-one

https://huagongshe.com/reaction/74994

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물TriethylamineHCID 8471—
반응물Trimethylsilyl triflateHCID 65367—
반응물1-Methylcyclohex-3-ene-1-carboximidic acidHCID 3052840—
용매DichloromethaneHCID 6344—
용매PentaneHCID 8003—
생성물4-Iodo-1-methyl-6-azabicyclo[3.2.1]octan-7-oneHCID 67286126—

반응 단계

A solution of 1-methylcyclohex-3-ene-1-carboxamide, 52b, (5.0 g, 35.9 mmol) dissolved in 100 mL of pentane and CH2Cl2 was cooled to 0° C. and treated with triethylamine (11.0 mL, 79.0 mmol) and trimethylsilyl-triflate (14.3 mL, 79.0 mmol) sequentially. The resulting mixture was stirred for 1 hour at room temperature. The lower layer was removed via pipette. The upper pentane layer was concentrated in vacuo and the resulting residue was dissolved in THF (100 mL). To the stirred reaction was added iodine (20.1 g, 79.02 mmol) and the reaction was allowed to stir overnight at room temperature. After quenching with Na2SO3 and NaHCO3, the reaction was partitioned between CH2Cl2 and water. The organic layers were combined, dried over Na2SO4, concentrated in vacuo to a dark yellow oil (9.5 g) that was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829007B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-77fac139931c443595455cd9f7021773
출처 메모uspto-grants-2014_09