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Water → 1-phenyl-N-(1,3-thiazol-2-ylmethyl)methanamine

HRID 651036
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HRID 651036 반응식
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[S:9]1[CH:13]=[CH:12][N:11]=[C:10]1[CH:14]=O.O>C1(C)C=CC=CC=1>[CH2:1]([NH:8][CH2:14][C:10]1[S:9][CH:13]=[CH:12][N:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 7504BenzylamineHCID 27349031,3-Thiazole-2-carbaldehyde

생성물 1

HCID 47776191-phenyl-N-(1,3-thiazol-2-ylmethyl)methanamine수율 58.9%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A stirred solution of N-benzylamine (0.56 mL, 5.1 mmol) and 2-thiazolecarboxaldehyde (0.55 g, 4.9 mmol) in toluene was heated to reflux for 2 hours with azeotropic removal of water. The solution was cooled to room temperature and concentrated to an oil. This oil was dissolved in 15 mL of ethanol and treated with excess NaBH4 and the mixture stirred overnight. Acetone was added and the mixture stirred 30 minutes and concentrated to a soild mass. This mass was partitioned between 2N aqueous NaOH and 2 portions of ethyl ether. The combined ethereal extracts were washed with water, brine, dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography on silica gel to provide 0.59 g (57%) of the title compound.

후처리

  1. concentrationconcentrated to an oil
  2. dissolutionThis oil was dissolved in 15 mL of ethanol
  3. additiontreated with excess NaBH4
  4. additionAcetone was added
  5. stirringthe mixture stirred 30 minutes
  6. concentrationconcentrated to a soild mass
  7. customThis mass was partitioned between 2N aqueous NaOH and 2 portions of ethyl ether
  8. washThe combined ethereal extracts were washed with water, brine
  9. dry with materialdried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customThe residue was purified by flash column chromatography on silica gel

출처 및 근거

ORD 기록
ord-74db08013dc7466199a32a173adbda77
출처 데이터셋
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06277871B1

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