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Diethyl Ether → 2-(3-Fluoro-4-methoxyphenyl)ethanamine

HRID 14860
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HRID 14860 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].C(OCC)C.[F:12][C:13]1[CH:18]=[C:17]([CH:19]=[CH:20][N+:21]([O-])=O)[CH:16]=[CH:15][C:14]=1[O:24][CH3:25]>C(OCC)(=O)C>[F:12][C:13]1[CH:18]=[C:17]([CH2:19][CH2:20][NH2:21])[CH:16]=[CH:15][C:14]=1[O:24][CH3:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 21226445Aluminium lithium hydrideHCID 534146392-Fluoro-1-methoxy-4-(2-nitro-vinyl)benzene

생성물 1

HCID 4263002-(3-Fluoro-4-methoxyphenyl)ethanamine

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Lithium aluminum hydride (200 mL of 1 M in diethyl ether) was placed in a 1 L round bottomed flask along with 300 mL of diethyl ether. Intermediate 81 was placed in the thimble of a soxhlet extractor atop this flask and the mixture refluxed for 24 hours. The mixture was cooled to ° 0 C and 50 mL of ethyl acetate added dropwise. After stirring for 1 hour, the mixture was quenched with 100 mL of 1 N KHSO4. The Organic layer was separated washed with sat. NaHCO3, sat. NaCl, and dried over MgSO4. Removal of the solvent gave product. LC-MS showed the product had the expected M+H+ of 170. It was used in the next step without purification.

후처리

  1. temperaturethe mixture refluxed for 24 hours
  2. temperatureThe mixture was cooled
  3. additionadded dropwise
  4. customthe mixture was quenched with 100 mL of 1 N KHSO4
  5. customThe Organic layer was separated
  6. washwashed with sat. NaHCO3, sat. NaCl
  7. dry with materialdried over MgSO4
  8. customRemoval of the solvent
  9. customgave product
  10. customIt was used in the next step without purification

출처 및 근거

ORD 기록
ord-723443a7ec354a99a1baf57c172e285f
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732444B2

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