Hydrochloric Acid → 2-Chlorodibenzo[b,f]oxepin-10(11h)-one

HRID 437817노트

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HRID 437817 반응식
N[C:2]1[CH:17]=[CH:16][C:5]2[O:6][C:7]3[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=3[C:9](=[O:11])[CH2:10][C:4]=2[CH:3]=1.CS(O)(=O)=O.N([O-])=O.[Na+].[ClH:27]>[Cu]Cl.C(OCC)(=O)C.O>[Cl:27][C:2]1[CH:17]=[CH:16][C:5]2[O:6][C:7]3[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=3[C:9](=[O:11])[CH2:10][C:4]=2[CH:3]=1

참가 물질

8

반응물 4

HCID 313Hydrochloric AcidHCID 6395Methanesulfonic AcidHCID 227679272-Amino-10,11-dihydro-dibenz[b,f]oxepin-10-oneHCID 23668193Sodium Nitrite

생성물 1

HCID 127651152-Chlorodibenzo[b,f]oxepin-10(11h)-one

시약·촉매·용매 3

HCID 62652Cuprous chloride촉매HCID 962Water용매HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

26.4 G. of 2-amino-10,11-dihydro-dibenz[b,f]oxepin-10-one are dissolved in 230 ml. of 2-N aqueous methanesulfonic acid. The mixture is cooled to 0° C. There is added dropwise thereto over a period of 7 minutes a solution of 10.7 g. of sodium nitrite in 37.5 ml. of water in such a manner that the temperature does not exceed 5° C. The mixture is stirred for an additional 5 minutes at 5° C. Then, this solution of the diazonium methanesulfonate is poured into a mixture of 500 ml. of ethyl acetate and a solution of 37.5 g. of copper (I) chloride in 450 ml. of concentrated hydrochloric acid. The resulting mixture is stirred for an additional 10 minutes at room temperature and the phases are then separated. The ethyl acetate solution is washed several times with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated in vacuo. The residue is dissolved in benzene and chromatographed over 400 g. of silica gel. Upon elution with benzene, there is obtained a substance which is crystallized from a small amount of isopropanol and there is obtained 2-chloro-10,11-dihydro-dibenz[b,f]oxepin-10-one having a melting point of 60°-61° C.

후처리

  1. additionThere is added dropwise
  2. customdoes not exceed 5° C
  3. stirringThe resulting mixture is stirred for an additional 10 minutes at room temperature
  4. customthe phases are then separated
  5. washThe ethyl acetate solution is washed several times with saturated aqueous sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. customevaporated in vacuo
  8. dissolutionThe residue is dissolved in benzene
  9. customchromatographed over 400 g
  10. washUpon elution with benzene
  11. customthere is obtained a substance which
  12. customis crystallized from a small amount of isopropanol

출처 및 근거

ORD 기록
ord-814f81996170462cada8b839ba26e9c5
출처 데이터셋
uspto-grants-1977_06
특허 번호
US04032525

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