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2,3,4,5-tetrahydro-1H-1-benzazepine → 313667-22-0

HRID 1266094
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HRID 1266094 반응식
[N:1]([O-:3])=O.[Na+].[NH:5]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH2:9][CH2:8][CH2:7][CH2:6]1>O.CC(O)=O>[N:1]([N:5]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH2:9][CH2:8][CH2:7][CH2:6]1)=[O:3]
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참가 물질

5

반응물 2

HCID 5765032,3,4,5-tetrahydro-1H-1-benzazepineHCID 23668193Sodium Nitrite

생성물 1

HCID 21859610313667-22-0수율 91%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

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온도
5 °C

실험 절차

A solution of sodium nitrite (1.35 g, 19.6 mmol) in water (4.0 mL) was added dropwise to a solution of 2,3,4,5-tetrahydro-1H-1-benzazepine (2.40 g, 16.3 mmol) in AcOH (10 mL) at 0-10° C. The mixture was stirred at 5° C. for 10 min, room temperature for 1 h and extracted with CH2Cl2 (3×20 mL). The organic layer was dried (MgSO4), concentrated in vacuo and flash column chromatography (EtOAc:hexane/1:9) gave 1-nitroso-2,3,4,5-tetrahydro-1H-1-benzazepine (2.60 g, 91%) as a brown liquid. 1H NMR (CDCl3, 300 MHz) δ1.70-1.85 (m, 4H), 2.70-2.82 (m, 2H), 3.92 (br, 2H), 7.25-7.32 (m, 1H), 7.32-7.40 (m, 2H), 7.40-7.48 (m, 1H) ppm.

후처리

  1. extractionextracted with CH2Cl2 (3×20 mL)
  2. dry with materialThe organic layer was dried (MgSO4)
  3. concentrationconcentrated in vacuo and flash column chromatography (EtOAc:hexane/1:9)

출처 및 근거

ORD 기록
ord-f22ed40170c9491fb2ffa5a06d0b207d
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06548493B1

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