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Bis(2-chloroethyl) ether → 4-(1H-Indol-6-yl)morpholine

HRID 2361236
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HRID 2361236 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH2:10])[CH:8]=2)[CH:3]=[CH:2]1.Cl[CH2:12][CH2:13][O:14][CH2:15][CH2:16]Cl.C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C.CCCCCC>CC(O)(C)C.C(OCC)(=O)C>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N:10]3[CH2:16][CH2:15][O:14][CH2:13][CH2:12]3)[CH:8]=2)[CH:3]=[CH:2]1
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참가 물질

7

반응물 4

HCID 8115Bis(2-chloroethyl) etherHCID 10340Sodium CarbonateHCID 2560966-AminoindoleHCID 21226206Ethyl acetate hexane

생성물 1

HCID 219558904-(1H-Indol-6-yl)morpholine수율 82.4%

시약·촉매·용매 2

HCID 6386tert-Butanol용매
HCID 8857
Ethyl Acetate
용매

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온도
100 °C

실험 절차

A mixture of 1H-indol-6-amine (3.14 g, 23.76 mmol), 1-chloro-2-(2-chloroethoxy)ethane (4.18 mL, 35.6 mmol), and sodium carbonate (10.07 g, 95 mmol) in t-BuOH (90 mL) was heated at 100° C. in a pressure tube for 3.5 days. On cooling to room temperature, the mixture was diluted with ethyl acetate and filtered through CELITE®. The filtrate was concentrated under vacuum to dryness. To the residue was added water (50 mL). The mixture was adjusted to pH 11 with saturated NaHCO3 solution and extracted with CH2Cl2 (4×80 mL). The combined extract was washed with brine (50 mL) and dried over anhydrous MgSO4. The desired product (3.96 g, 19.58 mmol, 82% yield) was isolated as a beige solid with ISCO (300 g silica gel, solid loading, 20-50% ethyl acetate/hexane).

후처리

  1. temperatureOn cooling to room temperature
  2. filtrationfiltered through CELITE®
  3. concentrationThe filtrate was concentrated under vacuum to dryness
  4. additionTo the residue was added water (50 mL)
  5. extractionextracted with CH2Cl2 (4×80 mL)
  6. extractionThe combined extract
  7. washwas washed with brine (50 mL)
  8. dry with materialdried over anhydrous MgSO4

출처 및 근거

ORD 기록
ord-ffbb58392a274cd18784196b490dea34
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08685969B2

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