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Hydrogen iodide → HCID 23455799、化合物

HRID 839171
ノート
印刷プレビュー

反応式

HRID 839171 の反応式
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]Br)=[CH:5][CH:4]=1.[IH:16]>C(O)(=O)C>[OH:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][I:16])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24841Hydrogen iodideHCID 10588171Benzene, 1-(6-bromohexyl)-4-methoxy-

生成物 1

HCID 23455799HCID 23455799、化合物

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A solution of 68 g. (0.25 mole) of 6-(4-methoxyphenyl)hexyl bromide in 500 ml. of glacial acetic acid was treated with 200 ml. of 50% aqueous hydriodic acid. The reaction was boiled at reflux for 5 hours. During the reflux period the condenser was removed briefly from time to time to allow methyl iodide to escape. The reaction was evaporated to dryness in vacuo. The residue was partitioned between water and ether. The organic phase was washed with water, then with dilute sodium thiosulfate until the iodine color was gone. The clear organic solution was evaporated in vacuo in a warm water bath to give a clear oil, 70 g. (92%) of 6-(4-hydroxyphenyl)hexyl iodide, which crystallized slowly after several days at room temperature.

後処理

  1. temperatureat reflux for 5 hours
  2. customDuring the reflux period the condenser was removed briefly from time to time
  3. customThe reaction was evaporated to dryness in vacuo
  4. customThe residue was partitioned between water and ether
  5. washThe organic phase was washed with water
  6. customThe clear organic solution was evaporated in vacuo in a warm water bath
  7. customto give a clear oil, 70 g
  8. custom(92%) of 6-(4-hydroxyphenyl)hexyl iodide, which crystallized slowly after several days at room temperature

出典と根拠

ORDレコード
ord-cfd3294fabf24187986afb9c44521d69
出典データセット
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04093736

反応ノート

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