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Sodium hydride → 3-Methoxy-N-(2-methoxyphenyl)-N-(2-tetrahydropyranyloxyethyl)benzamide

HRID 2462
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인쇄 미리보기

반응식

HRID 2462 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:17]=[CH:18][CH:19]=1)[C:6]([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15][CH3:16])=[O:7].[H-].[Na+].[O:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH:23]1[O:28][CH2:29][CH2:30]Br>CN(C=O)C>[O:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH:23]1[O:28][CH2:29][CH2:30][N:8]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15][CH3:16])[C:6](=[O:7])[C:5]1[CH:17]=[CH:18][CH:19]=[C:3]([O:2][CH3:1])[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 866212-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 9028663-methoxy-N-(2-methoxyphenyl)benzamide

생성물 1

HCID 539260843-Methoxy-N-(2-methoxyphenyl)-N-(2-tetrahydropyranyloxyethyl)benzamide수율 67%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

In an atmosphere of argon, 3-methoxy-N-(2-methoxyphenyl) benzamide (500 mg, 1.94 mmol) was dissolved in DMF (10 ml) to which was subsequently added sodium hydride (85 mg, 60%, 2.13 mmol) at room temperature, followed by 20 minutes of stirring. After additional 5 minutes of stirring under an ultrasonic irradiation condition at the same temperature, to this was added 2-tetrahydropyranyloxyethyl bromide (446 mg, 2.13 mmol) at room temperature. After 1 hour of stirring at room temperature and subsequent stirring at 70° C. for 6 hours, DMF was removed by evaporation, and the resulting residue was mixed with water (20 ml), extracted with ether and then washed with water and saturated brine. The resulting organic layer was dried on anhydrous magnesium sulfate, the solvent was removed by evaporation and then the resulting orange oily residue was purified by subjecting it to a silica gel column chromatography (ether:hexane=2:1) to obtain 501 mg (67.0%) of the title compound in the form of yellow oil.

후처리

  1. customat room temperature
  2. stirringAfter additional 5 minutes of stirring under an ultrasonic irradiation condition at the same temperature
  3. stirringAfter 1 hour of stirring at room temperature
  4. stirringsubsequent stirring at 70° C. for 6 hours
  5. customDMF was removed by evaporation
  6. additionthe resulting residue was mixed with water (20 ml)
  7. extractionextracted with ether
  8. washwashed with water and saturated brine
  9. dry with materialThe resulting organic layer was dried on anhydrous magnesium sulfate
  10. customthe solvent was removed by evaporation
  11. customthe resulting orange oily residue was purified

출처 및 근거

ORD 기록
ord-3ded3b8d2ed540a4b76f3f398d06c312
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05728835

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