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1-Bromo-3-chloropropane → 1-[4-(3-Chloropropoxy)-3-methylphenyl]ethanone

HRID 1193649
ノート
印刷プレビュー

反応式

HRID 1193649 の反応式
[CH3:1][C:2]1[CH:7]=[C:6]([C:8]([CH3:10])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:11].Br[CH2:13][CH2:14][CH2:15][Cl:16].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Cl:16][CH2:15][CH2:14][CH2:13][O:11][C:3]1[CH:4]=[CH:5][C:6]([C:8](=[O:9])[CH3:10])=[CH:7][C:2]=1[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 80061-Bromo-3-chloropropaneHCID 11430Potassium CarbonateHCID 701354'-Hydroxy-3'-methylacetophenone

生成物 1

HCID 144071751-[4-(3-Chloropropoxy)-3-methylphenyl]ethanone収率 95.1%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A mixture of 25 g (0.166 mole) of 4-hydroxy-3-methylacetophenone, 45.8 g (0.33 mole) of 1-bromo-3-chloropropane and 69.1 g (0.5 mole) of anhydrous potassium carbonate in 500 ml of acetone was heated at reflux for 20 hr. The mixture was cooled, filtered, and the filtrate concentrated under reduced pressure to give an oil as residue. The oil was crystallized in petroluem ether. The solid was collected by filtration, washed with petroleum ether and dried to yield 35.8 g (95%) of an off-white powder. An analytical sample, m.p. 41.5°-42.5° C. was prepared from petroleum ether.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 20 hr
  3. temperatureThe mixture was cooled
  4. filtrationfiltered
  5. concentrationthe filtrate concentrated under reduced pressure
  6. customto give an oil as residue
  7. customThe oil was crystallized in petroluem ether
  8. filtrationThe solid was collected by filtration
  9. washwashed with petroleum ether
  10. customdried

出典と根拠

ORDレコード
ord-829dc3e901ef4d2dac2b82cc6015a0ee
出典データセット
uspto-grants-1989_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04810713

反応ノート

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