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Acetic Acid → Phenol, 4-(2,2-dichloroethenyl)-

HRID 482858
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HRID 482858 반응식
O1CCCCC1O[C:8]1[CH:9]=[C:10]([CH:14](OC(=O)C)[C:15]([Cl:18])(Cl)[Cl:16])[CH:11]=[CH:12][CH:13]=1.C(O)(=[O:25])C>[Zn]>[Cl:16][C:15]([Cl:18])=[CH:14][C:10]1[CH:11]=[CH:12][C:13]([OH:25])=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 176Acetic AcidHCID 13324246HCID 13324246, 화합물

생성물 1

HCID 5324901Phenol, 4-(2,2-dichloroethenyl)-

시약·촉매·용매 1

HCID 23994Zinc촉매

실험 절차

22 g (0.06 mole) of 3-(tetrahydropyranyloxy)-1-(2,2,2-trichloro-1-acetoxyethyl)-benzene were dissolved in 80 ml of glacial acetic acid, 4.6 g (0.07 mole) of zinc dust were added a little at a time, and the mixture was heated at 60°-70° C. for 3 hours. The mixture was cooled and filtered, after which it was introduced into 1.5 liters of water and extracted with ether. The extracts were combined, washed three times with NaHCO3 solution and water, dried end evaporated down, and the residue was taken up in toluene. The solution was filtered over silica gel, and 8.0 g of 4-dichlorovinylphenol were obtained as a wax-like product.

후처리

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  1. temperaturethe mixture was heated at 60°-70° C. for 3 hours
  2. temperatureThe mixture was cooled
  3. filtrationfiltered
  4. additionafter which it was introduced into 1.5 liters of water
  5. extractionextracted with ether
  6. washwashed three times with NaHCO3 solution and water
  7. customdried end
  8. customevaporated down
  9. filtrationThe solution was filtered over silica gel

출처 및 근거

ORD 기록
ord-1d50582121f442ecbe772e253b86d310
출처 데이터셋
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04576935

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