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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Carbonic Acid → 2-Hydroxy-2,4-dimethyl-3-pentanone

HRID 462852
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HRID 462852 반응식
[CH3:1][CH:2]([C:4](=[O:8])[CH:5]([CH3:7])[CH3:6])[CH3:3].BrBr.[OH:11]C(O)=O>C(Cl)(Cl)Cl>[OH:11][C:2]([CH3:3])([C:4](=[O:8])[CH:5]([CH3:7])[CH3:6])[CH3:1]
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참가 물질

5

반응물 3

HCID 767Carbonic AcidHCID 112712,4-Dimethyl-3-pentanoneHCID 24408Bromine

생성물 1

HCID 5477352-Hydroxy-2,4-dimethyl-3-pentanone

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

To a stirred solution of 28.3 ml. (0.2 mole) 2,4-dimethyl-3-pentanone in 100 ml. chloroform was added dropwise 10.3 ml. (0.2 mole) bromine in 30 ml. of the same solvent. The resulting mixture was stirred for a few minutes, the solvent evaporated in vacuo, the residue taken up in 100 ml. ethanol. Water, 50 ml., and 10M sodium hydroxide, 50 ml., added. The resulting mixture was stirred at reflux for one hour, diluted with 200 ml. water and extracted with 3×50 ml. ethyl ether. The extracts were dried (MgSO4) evaporated to dryness and the residue distilled to obtain 15.95 g. (61%) of the hydroxy-ketone, b.p. 60°-62° C./18 mm.

후처리

  1. customthe solvent evaporated in vacuo
  2. addition, added
  3. stirringThe resulting mixture was stirred
  4. temperatureat reflux for one hour
  5. additiondiluted with 200 ml
  6. extractionwater and extracted with 3×50 ml
  7. dry with materialThe extracts were dried (MgSO4)
  8. customevaporated to dryness
  9. distillationthe residue distilled
  10. customto obtain 15.95 g

출처 및 근거

ORD 기록
ord-ad19b98b26ab455d96f59a3212d79208
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04517379

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