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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen iodide → HCID 23455799, 화합물

HRID 839171
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HRID 839171 반응식
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
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참가 물질

4

반응물 2

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

생성물 1

HCID 23455799HCID 23455799, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-cfd3294fabf24187986afb9c44521d69
출처 데이터셋
uspto-grants-1978_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04093736

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