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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Phosphoric Acid → HCID 66920177, 화합물

HRID 1510073
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HRID 1510073 반응식
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[N:13]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14]1.ClN1C(=[O:28])CCC1=O.P(=O)(O)(O)O>C(Cl)Cl.O>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[N:13]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:15][C:14]1=[O:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 1004Phosphoric AcidHCID 31398ChlorosuccinimideHCID 66920309HCID 66920309, 화합물

생성물 1

HCID 66920177HCID 66920177, 화합물수율 72.8%

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매

실험 절차

The compound of step 2 (3.09 g, 11.0 mmol) was dissolved in DCM (83 ml), and N-chlorosuccinimide (1.54 g, 11.6 mmol) was added. The reaction mixture was stirred at room temperature for 2 h. The solvent was removed, the resulting solid was dissolved in concentrated acetic acid (45 ml) and heated to 70° C. After the addition of phosphoric acid (9.35 ml, 137 mmol; 85%), the reaction mixture was heated to 120° C. for 2 h. The cooled mixture was diluted with water, extracted with EA, the organic layer separated, dried over sodium sulfate, filtered, and evaporated. The residue was purified by silica gel chromatography (EA/HEP 1:6). 2.38 g of the title compound was obtained.

후처리

  1. customThe solvent was removed
  2. dissolutionthe resulting solid was dissolved in concentrated acetic acid (45 ml)
  3. temperatureheated to 70° C
  4. temperaturethe reaction mixture was heated to 120° C. for 2 h
  5. extractionextracted with EA
  6. customthe organic layer separated
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue was purified by silica gel chromatography (EA/HEP 1:6)

출처 및 근거

ORD 기록
ord-df05b4478fde472aa197bd25095dfa54
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211885B2

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