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Water → [3-(Aminomethyl)phenyl]methanol

HRID 416686
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HRID 416686 반응식
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[C:6]#[N:7].[H-].[H-].[H-].[H-].[Li+].[Al+3].O>C1COCC1>[NH2:7][CH2:6][C:5]1[CH:4]=[C:3]([CH:10]=[CH:9][CH:8]=1)[CH2:2][OH:1]
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참가 물질

5

반응물 3

HCID 962WaterHCID 27346773-(Hydroxymethyl)benzonitrileHCID 21226445Aluminium lithium hydride

생성물 1

HCID 21880609[3-(Aminomethyl)phenyl]methanol수율 40%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 3-(hydroxymethyl)benzonitrile in THF was slowly added to a refluxing solution of LiAlH4 in THF with vigorous stirring, maintained under nitrogen atmosphere. The solution was heated at reflux overnight and water was thereafter slowly added dropwise to quench the reaction (until no further evolution of H2 was apparent). The THF was evaporated under reduced pressure and ether/acidified water was added. The ether phase was discarded. The aqueous phase was washed with ether and the organic phase was discarded. NaOH was added until the pH of the aqueous phase reached pH 7. The solution was extracted with THF three times, dried over MgSO4 and evaporated under reduced pressure to furnish a slightly yellow residue which was purified by chromatography on a silica gel column using a gradient eluent starting from ethyl acetate and ending with a mixture of 1:1 ethyl acetate:MeOH), to give the intermediate in a 40% yield.

후처리

  1. temperaturemaintained under nitrogen atmosphere
  2. temperatureThe solution was heated
  3. temperatureat reflux overnight
  4. customto quench
  5. customthe reaction (until no further evolution of H2
  6. customThe THF was evaporated under reduced pressure and ether/
  7. additionwas added
  8. washThe aqueous phase was washed with ether
  9. additionNaOH was added until the pH of the aqueous phase
  10. extractionThe solution was extracted with THF three times
  11. dry with materialdried over MgSO4
  12. customevaporated under reduced pressure
  13. customto furnish a slightly yellow residue which
  14. customwas purified by chromatography on a silica gel column
  15. additionending with a mixture of 1:1 ethyl acetate
  16. customMeOH), to give the intermediate in a 40% yield

출처 및 근거

ORD 기록
ord-975406b824224c50944eb6894d13a310
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08088941B2

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