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Morpholine → 2-Methoxy-5-morpholin-4-ylmethyl-benzonitrile

HRID 1167328
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HRID 1167328 반응식
Cl[CH2:2][C:3]1[CH:4]=[CH:5][C:6]([O:11][CH3:12])=[C:7]([CH:10]=1)[C:8]#[N:9].[NH:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1>O1CCCC1>[CH3:12][O:11][C:6]1[CH:5]=[CH:4][C:3]([CH2:2][N:13]2[CH2:18][CH2:17][O:16][CH2:15][CH2:14]2)=[CH:10][C:7]=1[C:8]#[N:9]
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참가 물질

4

반응물 2

HCID 8083MorpholineHCID 229961915-(Chloromethyl)-2-methoxybenzonitrile

생성물 1

HCID 229962172-Methoxy-5-morpholin-4-ylmethyl-benzonitrile수율 99%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 5-chloromethyl-2-methoxy-benzonitrile (246 mg, 1.354 mmol, example 29) in tetrahydrofuran (10 mL) at room temperature was added morpholine (1.193 mL, 13.54 mmol). The reaction mixture was heated at reflux for 4 h. The reaction was concentrated in vacuo (with heating) to remove morpholine and tetrahydrofuran to afford 2-methoxy-5-morpholin-4-ylmethyl-benzonitrile as a yellow oil (311.2 mg, 99%). The crude product was used without further purification.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 4 h
  3. concentrationThe reaction was concentrated in vacuo (with heating)
  4. customto remove morpholine and tetrahydrofuran

출처 및 근거

ORD 기록
ord-6bebd5ab91ac4184938f0debdedbeb45
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06617346B1

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