돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1415282생성일: 2026년 10월 27일

Acetaldehyde → 1-(3,3-Diphenylureido)ethylphosphonic acid

https://huagongshe.com/reaction/1415282

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물Carbon DioxideHCID 280—
반응물Triphenyl phosphiteHCID 7540—
반응물1,1-DiphenylureaHCID 33603—
반응물PhosphiteHCID 107908—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물1-(3,3-Diphenylureido)ethylphosphonic acidHCID 21423551—

반응 단계

Freshly distilled acetaldehyde (0.22 mole) is added during 0.5 hr to a stirred solution of 0.1 mole each of 1,1-diphenylurea and triphenyl phosphite in 130g of benzene at 60° C. The solution is warmed at reflux (65°-70° with a Dry Ice-cooled condenser) for 1.25 hr, giving a dark brown solution having a small 31P nmr peak at -126.2 ppm for unrected phosphite and a large product peak at -18.4 ppm (~1:5 areas). The reaction mixture is stripped to 130°/3mm and the residue diluted with 200 ml of acetonitrile and 10g of H2O, and this solution warmed at reflux for 3 hr. Solid that separates during warming is recrystallized from acetic acid-water to give the product as a white solid: mp 186°-187° C dec; P31 nmr -21.6 ppm; 1H nmr δ10.0 (s, 2, OH), 7.3 (m, 10, C6H5), 5.4 (d of d, 1, J = 9 and 5Hz, NH), 4.1 (m, 1, CH), 1.3 (d, of d, 3, J = 16 and 7 Hz, CH3); acidity 2.00 equiv/mole, pK1 = 2.20, pK2 = 8.62.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04003965
출처 데이터셋uspto-grants-1977_01
ORD IDord-89a33b6793d546c3b360885512ce11d6
출처 메모uspto-grants-1977_01