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Toluene → 5,6-dichloro-1H-indene

HRID 2226533
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HRID 2226533 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[Cl:11])[CH:7](O)[CH2:6][CH2:5]2.C1(C)C=CC=CC=1.C1(C)C=CC(S(O)(=O)=O)=CC=1.[OH-].[Na+]>O.C(C1C=C(O)C(=CC=1)O)(C)(C)C>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[Cl:11])[CH2:7][CH:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 1140TolueneHCID 6101p-Toluenesulfonic acidHCID 14798Sodium HydroxideHCID 199195245,6-Dichloro-2,3-dihydro-1H-inden-1-OL

생성물 1

HCID 199195275,6-dichloro-1H-indene수율 56.5%

시약·촉매·용매 2

HCID 73814-tert-Butylcatechol촉매

실험 절차

A mixture of 17.48 g of the product of Step B, 470 ml of toluene, 0.57 g of 4-tert.-butyl-catechol and 1.63 g of p-toluene sulfonic acid was refluxed for 2 hours and then was diluted with water. 10 ml of N sodium hydroxide solution were added and the mixture was extracted with toluene. The organic phase was evaporated to dryness under reduced pressure and the residue was taken up in hexane. The mixture was vacuum filtered and the crystalline product was dried to obtain 9 g of the desired product melting at 76° C.

후처리

  1. temperaturewas refluxed for 2 hours
  2. extractionthe mixture was extracted with toluene
  3. customThe organic phase was evaporated to dryness under reduced pressure
  4. filtrationfiltered
  5. customthe crystalline product was dried

출처 및 근거

ORD 기록
ord-697626cccf67485283f663d344ef5127
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05348971

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HCID 962
Water
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