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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48870생성일: 2026년 10월 25일

Dimethyl Sulfoxide → HCID 22715291, 화합물

https://huagongshe.com/reaction/48870

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물PyridineHCID 1049—
반응물4'-Chloroacetyl(acetanilide)HCID 8805—
용매Diethyl EtherHCID 3283—
생성물HCID 22715291HCID 22715291—

반응 단계

A solution of 2.12 g of 4-acetaminophenacyl chloride, 0.83 g of pyridine, and 6.4 g of dimethyl sulfoxide was agitated for one night. 0.8 g of pyridine and 1 g of dimethyl sulfoxide were further added, and thereafter, the resulting solution was further agitated for 5 hours. 50 mL of ether was added, and acetamidophenacylpyridinium chloride was separated by filtration. The separated acetamidophenacylpyridinium chloride was dissolved into water, and the resulting solution was filtered, and thereafter, 1.7 g of concentrated nitric acid was added. The resulting solution was boiled for one hour, and after cooling, acetone was added. Then, 4-aminophenacylpyridinium chloride hydrochloride was produced by filtration. 2 g of the resulting 4-aminophenacylpyridinium chloride hydrochloride was dissolved into 15 g of water, and 4.5 g of basic ion-exchange resin (Amberlite IRA400-OH) was added. After agitation, the ion-exchange resin was removed by filtration so as to produce an aqueous solution of 4-aminophenacylpyridinium chloride. An aqueous solution of 25 g of water and 1.3 g of 4-aminophenacylpyridinium chloride was refluxed with 1 g of silver nitrate for 90 minutes. Generated precipitates were removed by filtration. Then, 5 g of carbon black having a specific surface area of 200 m2/g and DBPA of 122 mL/100 g was added, and the resulting mixture was heated to about 80° C. 0.52 g of concentrated hydrochloric acid was added, and thereafter, a solution of small amounts of water and sodium nitrite was added. Furthermore, the disperse liquid was agitated for 1.5 hours. As a consequence, a diazonium salt including NN+C6H4COCH2(N+C5H5) group having the following structure was produced and was reacted with carbon black. As a result, a product in which C6H4COCH2(N+C5H5) group was bound to the surface of the carbon black was produced. The resulting carbon black powder was dispersed in water again, so as to produce a self-dispersing carbon black disperse material having a pigment content of 15%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706105B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-7d7d1d3062a849a9a07a1eb8076d4871
출처 메모uspto-grants-2004_03