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Acetic Acid → (RS)-4-[(methyl-phenethyl-amino)-methyl]-3,4-dihydro-2H-benzo[b]oxepin-5-one

HRID 849674
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인쇄 미리보기

반응식

HRID 849674 반응식
Cl.[CH3:2][NH:3][CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[CH2:12]=[O:13].[C:14]([OH:17])(=O)[CH3:15]>>[CH3:2][N:3]([CH2:8][CH:9]1[CH2:10][CH2:11][O:17][C:14]2[CH:15]=[CH:4][CH:5]=[CH:6][C:7]=2[C:12]1=[O:13])[CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 176Acetic AcidHCID 712FormaldehydeHCID 77742Methyl(2-phenylethyl)amine hydrochloride

생성물 1

HCID 19367697(RS)-4-[(methyl-phenethyl-amino)-methyl]-3,4-dihydro-2H-benzo[b]oxepin-5-one

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온도
100 °C

실험 절차

A mixture of 24.4 g 3,4-dlihydro-2H-benzo[b]oxepin-5-one, 17.2 g N-methyl-2-phenylethylamine hydrochloride and 3.0 g paraformaldehyde in 200 ml glacial acetic acid was heated at 100° C. for 3 hours. Thereafter, the solvent was evaporated under vacuum and the residue was taken up in 200 ml water. The product was extracted three times with 100 ml diethyl ether each time. The aqueous phase was made alkaline with potassium carbonate and was extracted three times with 100 ml dichloromethane each time. After washing the extracts with saturated sodium chloride solution, drying them over sodium sulphate and concentrating them by evaporation under vacuum, 23.9 g (77.2% theoretical) of the title compound remained behind as a yellowish oil.

후처리

  1. customThereafter, the solvent was evaporated under vacuum
  2. extractionThe product was extracted three times with 100 ml diethyl ether each time
  3. extractionwas extracted three times with 100 ml dichloromethane each time
  4. washAfter washing the extracts with saturated sodium chloride solution
  5. dry with materialdrying them over sodium sulphate
  6. concentrationconcentrating them
  7. customby evaporation under vacuum, 23.9 g (77.2% theoretical) of the title compound

출처 및 근거

ORD 기록
ord-ff7c2da586de4889bd7bbd57e06513fb
출처 데이터셋
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06013809

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