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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethyl phosphite → Phosphonic acid, [(formylamino)methyl]-, diethyl ester

HRID 905162
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HRID 905162 반응식
O[CH2:2][NH:3][CH:4]=[O:5].[CH2:6]([O:8][P:9]([O:13]CC)[O:10][CH2:11][CH3:12])[CH3:7]>C(O)C>[CH2:6]([O:8][P:9]([CH2:2][NH:3][CH:4]=[O:5])(=[O:13])[O:10][CH2:11][CH3:12])[CH3:7]
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참가 물질

4

반응물 2

HCID 31215Triethyl phosphite2회HCID 83086N-(Hydroxymethyl)formamide

생성물 1

HCID 12673118Phosphonic acid, [(formylamino)methyl]-, diethyl ester

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The mole ratio of N-(hydroxymethyl)formamide to triethylphosphite in step (2) of the process of the invention is 1:1. The reaction is conducted in the presence of heat and at a temperature sufficient to cause the reaction to go to completion. The reactants are heated until ethyl alcohol starts to evolve and this occurs at reflux temperature. When triethylphosphite is used, this temperature is approximately 120°-125° C. At this point, the alcohol is distilled off, leaving the product diethyl-N-(formyl)aminomethylphosphonate as the residue.

후처리

  1. temperatureof heat and at a temperature sufficient
  2. customthe reaction
  3. temperatureat reflux temperature
  4. customis approximately 120°-125° C
  5. distillationAt this point, the alcohol is distilled off

출처 및 근거

ORD 기록
ord-7133614b944b452fbfa4482758121e65
출처 데이터셋
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04422982

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