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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326787생성일: 2026년 10월 25일

Carbon Dioxide → (2,6-Dimethyl-4-[phenylacetamido]phenylsulfonyl)nitromethane

https://huagongshe.com/reaction/326787

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Phenylacetyl chlorideHCID 7679—
반응물Calcium CarbonateHCID 10112—
반응물Ici 222155HCID 195716—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(2,6-Dimethyl-4-[phenylacetamido]phenylsulfonyl)nitromethaneHCID 992892154%

반응 단계

Phenylacetyl chloride (1.16 g, 7.5 mM) was added to a stirred suspension of calcium carbonate (1.0 g, 10.0 mM) and (4-amino-2,6-dimethylphenylsulfonyl)nitromethane (1.22g, 5.0 mM) in dry tetrahydrofuran (THF; 20 mL). The mixture was stirred for 16 hours during which time carbon dioxide was slowly released. Ethanol (1.0 mL) was then added and the mixture stirred for a further hour in order to decompose excess phenylacetyl chloride. Ethyl acetate (100 mL) was then added and the insoluble material removed by filtration. The filtrate was washed first with water (50 mL) containing 2M hydrochloric acid (2.0 mL) and then with saturated sodium chloride solution (2×40 mL) and then dried (MgSO4). The solvent was evaporated and the residue recrystallised from ethyl acetate. The solid obtained was washed with ether and air dried to give (2,6-dimethyl-4-[phenylacetamido]phenylsulfonyl)nitromethane as white crystals, having m.p. 158°-159° C. and in 54 % yield after recrystallisation from ethanol; microanalysis, found: C, 56.7; H, 5.0; N, 8.0%; C17H18N2O5S requires: C, 56.4: H, 5.0; N, 7.7%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05270342
출처 데이터셋uspto-grants-1993_12
ORD IDord-da9f480164f94d9599cd4275cfc57a51
출처 메모uspto-grants-1993_12