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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239301생성일: 2026년 10월 25일

Diethyl Ether → N-(4-aminocyclohexyl)methanesulfonamide

https://huagongshe.com/reaction/239301

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Trifluoroacetic acidHCID 6422—
반응물N-[cis-4-(Boc-amino)cyclohexyl]methanesulfonamideHCID 18348373—
용매DichloromethaneHCID 6344—
생성물N-(4-aminocyclohexyl)methanesulfonamideHCID 18348422154.9%

반응 단계

1,1-Dimethylethyl {4-[(methylsulfonyl)amino]cyclohexyl}carbamate (0.922 g, 3.15 mmol) was dissolved in DCM (50 mL). TFA was added (2.429 mL, 31.5 mmol) and the reaction allowed to stir at rt for 1 h. Evaporated off the volatiles and added DCM (50 mL) followed by evaporation of volatiles. The DCM addition/evaporation was repeated several times to give a maroon semi-solid. The residual semi-solid was treated with diethyl ether (10 mL) after which the suspension was sonicated and triturated, then filtered. Solids were triturated with more diethyl ether (10 mL). The product was suction dried to give title compound of Step B as a light pink solid (0.938 g). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.80 (br. s., 2H), 7.07 (d, J=7.2 Hz, 1H), 3.33 (s, 2H), 3.01-3.14 (m, 1H), 2.78-3.01 (m, 2H), 1.80-2.02 (m, 4H), 1.17-1.47 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642759B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-ce550eb4d5f54eb8b6356e569550a51e
출처 메모uspto-grants-2014_02