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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 13708665, 화합물

HRID 1585535
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HRID 1585535 반응식
[C:1]1([CH2:7][C:8]([O-:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[K+].O.[CH:13]([Cl:16])(Cl)Cl>CN(C)C=O>[Cl:16][C:13]1[CH:5]=[CH:6][C:1]([C:7]2[CH2:8][O:9][C:8](=[O:10])[C:7]=2[C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:2][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6212ChloroformHCID 23675783Potassium phenylacetate

생성물 1

HCID 13708665HCID 13708665, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2-bromine-1-(4-chlorophenyl)-ethanone (2, 102.6 g, 0.44 mol) and potassium phenylacetate (1, 104.5 g, 0.6 mol) are heated to 80° C. in dimethyl formamide (600 mL) while being stirred for 4 hours and are then cooled. After the addition of water (1 L), chloroform is used for extraction (3 times 300 mL), and the chloroform extract is washed with water and then dried (Na2SO4) and concentrated to dryness. For crystallization, diisopropyl ether is added (500 mL) and the crystals, which are formed in the cold [and have] a melting point of 111-113° C., are collected (yield 92 g, 78% with reference to 2).

후처리

  1. temperatureare then cooled
  2. extractionis used for extraction (3 times 300 mL)
  3. extractionthe chloroform extract
  4. washis washed with water
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated to dryness
  7. customFor crystallization, diisopropyl ether
  8. additionis added (500 mL)
  9. customthe crystals, which are formed in the cold [and have] a melting point of 111-113° C.
  10. customare collected (yield 92 g, 78% with reference to 2)

출처 및 근거

ORD 기록
ord-aebd91ea28d849899d324c9b09005b91
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05939415

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