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Ethyl chloroacetate → HCID 70530867, 화합물

HRID 1155363
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HRID 1155363 반응식
[CH3:1][C:2]1[CH:15]=[CH:14][C:5]([S:6][C:7]2[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:22]([O:24][C:25](=[O:28])[CH2:26]Cl)[CH3:23]>CC(CC)=O>[CH2:22]([O:24][C:25](=[O:28])[CH2:26][O:13][C:10]1[CH:11]=[CH:12][C:7]([S:6][C:5]2[CH:14]=[CH:15][C:2]([CH3:1])=[CH:3][CH:4]=2)=[CH:8][CH:9]=1)[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7751Ethyl chloroacetateHCID 11430Potassium CarbonateHCID 123413444-[(4-Methylphenyl)sulfanyl]phenol

생성물 1

HCID 70530867HCID 70530867, 화합물수율 63.3%

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

While stirring, 30 g of 4(4-methylthio-phenoxy)-phenol were dissolved in 350 ml of methylethyl-ketone. After addition of 18 g of potassium carbonate and 16 g of chloroacetic acid ethyl ester, the mixture was heated at the boil for 8 hours. Inorganic components were then separated by suction-filtration. After vaporization of the organic solvent, the residue was dissolved in 300 ml of methylene chloride and the solution was shaken several times with water. The organic phase was vaporized and the residue was distilled in vacuo. 25 g of 4(4-methylthio-phenoxy)-phenoxy-acetic acid ethyl ester were obtained, boiling point: 215°-230°/3-4 mm mercury.

후처리

  1. temperaturethe mixture was heated at the boil for 8 hours
  2. customInorganic components were then separated by suction-filtration
  3. dissolutionAfter vaporization of the organic solvent, the residue was dissolved in 300 ml of methylene chloride
  4. stirringthe solution was shaken several times with water
  5. distillationthe residue was distilled in vacuo

출처 및 근거

ORD 기록
ord-58dba63818d34d6b8c4e6be6411a12f0
출처 데이터셋
uspto-grants-1981_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04301295

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