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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1447329생성일: 2026년 10월 27일

Lauric Acid → Nonanoic Acid

https://huagongshe.com/reaction/1447329

반응식

참여 물질

역할이름HCID투입량
반응물Lauric AcidHCID 3893—
반응물Lauryl alcohol diphosphonic acidHCID 4395717—
반응물Dodecane-1,1,2-triphosphonic acidHCID 20550621—
용매Phosphoric AcidHCID 1004—
용매Dibutyl butylphosphonateHCID 6539—
생성물Nonanoic AcidHCID 8158—

반응 단계

In similar manner C9, C12, C16 and C18 extractants were prepared at 150° C. from iso-nonanoic, lauric, iso-hexadecanoic and stearic acids respectively. NMR analysis of the C12 extractant revealed that dodecane-1,1,2-triphosphonic acid was a major component of the crude product and that 1-hydroxy-1,1-dodecane diphosphonic acid was absent. When a solution of the crude C12 extractant (10 wt %) in dibutyl butylphosphonate (10 wt %) and kerosene (80 wt %) was shaken with equal volume of 10 M phosphoric acid, the total carbon in the phosphoric acid was 0.01%. The same amount of carbon was found when a 10 wt % kerosene solution of dibutyl butyl phosphonate was used instead. These results indicate that loss of material from the crude C12 extractant during contact with phosphoric acid is negligible. A C12 extractant was also made from lauric acid by reaction at 110° C. for 16 h. The main component of this acid extractant was 1-hydroxy-1,1 -dodecanediphosphonic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04316877
출처 데이터셋uspto-grants-1982_02
ORD IDord-74634f1cc7ae49c980958fde48f33f85
출처 메모uspto-grants-1982_02