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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetone → Cimadronate

HRID 1576058
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HRID 1576058 반응식
[CH:1]1([NH:7][CH:8]=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[P:10]([OH:13])([OH:12])[OH:11].P(Cl)(Cl)Cl.CC(C)=O>O>[CH:1]1([NH:7][CH:8]([P:10]([OH:13])(=[O:11])[OH:12])[P:10]([OH:13])(=[O:12])[OH:11])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
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참가 물질

6

반응물 4

HCID 180AcetoneHCID 13017CyclohexylformamideHCID 24387Phosphorus trichlorideHCID 107909Phosphorous acid

생성물 1

HCID 405386Cimadronate수율 25%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

127.2 parts of N-cyclohexylformamide and 81 parts of phosphorous acid were reacted with 137.3 parts of phosphorus trichloride at 70°C, and maintained for 5 hours at this temperature. The reaction product was dissolved in water, treated with acetone and the precipitate separated. A 25% yield of N-cyclohexyl-1-aminomethane-1,1-diphosphonic acid, based on PCl3, was obtained.

후처리

  1. temperaturemaintained for 5 hours at this temperature
  2. customthe precipitate separated

출처 및 근거

ORD 기록
ord-bfae2ae7ca024e7ab7ce950696b3cb16
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03979385

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