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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263358생성일: 2026년 10월 27일

Carbon Dioxide → N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosourea

https://huagongshe.com/reaction/263358

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Carbonic AcidHCID 767—
반응물D-GlucoseHCID 5793—
반응물GlucopyranosylamineHCID 193433—
반응물o-nitrophenyl N-(2-chloroethyl)N-nitrosocarbamateHCID 13231923—
용매BenzeneHCID 241—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물N-(2-Chloroethyl)-N'-beta-D-glucopyranosyl-N-nitrosoureaHCID 997289186.8%

반응 단계

1.79 g (10 mmol) of 1-amino-1-deoxy-β-D-glucopyranose is dissolved (partially suspended) in 40 ml of anhydrous ethanol, and the solution is cooled to 0°-5° C. To this solution is added 2.2 g (50 mmol) of dry-ice little by little so as to convert the glucopyranose into its carbonic acid-addition salt. This acid-addition salt solution is then added dropwise to a solution prepared by dissolving 3.28 g (12 mmol) of o-nitrophenyl N-(2-chloroethyl)-N-nitrosocarbamate in a mixture of 40 ml anhydrous tetrahydrofuran and 10 ml benzene, while stirring, at 0°-5° C. over an hour. The resultant mixture is stirred further at 20°-25° C. for 2 hours, and the thus reacted solution is concentrated at 50° C. and below, under reduced pressure. The crystalline residue obtained is washed with anhydrous ethyl ether and then with acetone, dried under reduced pressure, and recrystallized from anhydrous isopropanol to give 2.72 g of 3-(β-D-glucopyranosyl)-1-(2 -chloroethyl)-1-nitrosourea. Yield 86.8%. mp 77°-78° C. (decomp.). [α]D25 -10.3° (C 1.0, water). Analysis for C9H16N3O7Cl (MW 313.69):

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04156777
출처 데이터셋uspto-grants-1979_05
ORD IDord-6c10161aca144d4da2bbe7f184dda8f1
출처 메모uspto-grants-1979_05