Iodine → 5-(3-iodopropyl)-5H-dibenzo[a,d]cycloheptene

HRID 1284229

반응식

HRID 1284229 반응식
C(O[CH2:4][CH2:5][CH2:6][C:7]1(O)[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[CH:11]=[CH:10][C:9]2[CH:18]=[CH:19][CH:20]=[CH:21][C:8]1=2)C.C(OC(=O)C)(=O)C.[IH:30].II>>[I:30][CH2:4][CH2:5][CH2:6][CH:7]1[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[CH:11]=[CH:10][C:9]2[CH:18]=[CH:19][CH:20]=[CH:21][C:8]1=2

참가 물질

5

반응물 4

HCID 807IodineHCID 7918Acetic AnhydrideHCID 24841Hydrogen iodideHCID 23328862HCID 23328862, 화합물

생성물 1

HCID 233288685-(3-iodopropyl)-5H-dibenzo[a,d]cycloheptene

반응 조건

온도
65 °C

실험 절차

A solution of 9.25 g. (0.0314 mole) of 5-(3-ethoxypropyl)-5-hydroxy-dibenzo[a,d]cycloheptene prepared as above in 45 ml. of acetic anhydride is heated on the steam-bath for 90 minutes then cooled to 65°C. A stream of nitrogen is passed through the solution while 30 ml. of hydriodic acid (sp. gr., 1.5) is added in portions, keeping the temperature below 90°C. The solution develops a dark brown iodine color during the addition. The solution is heated to 80°C. for 30 minutes, then cooled and poured into ice-water. The brown oil that separates is extracted into benzene and the extract washed with water, dilute sodium thiosulfate solution and finally with water. Evaporation of the benzene gives the product 5-(3-iodopropyl)-5H-dibenzo[a,d]cycloheptene as a yellow oil. A sample gives a precipitate with alcoholic silver nitrate solution.

후처리

  1. customthe temperature below 90°C
  2. additionduring the addition
  3. temperatureThe solution is heated to 80°C. for 30 minutes
  4. temperaturecooled
  5. extractionThe brown oil that separates is extracted into benzene
  6. washthe extract washed with water, dilute sodium thiosulfate solution and finally with water
  7. customEvaporation of the benzene

출처 및 근거

ORD 기록
ord-c513c1fe2498427f8684e5bd10a21bab
출처 데이터셋
uspto-grants-1976_08
특허 번호
US03978121

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