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3-Chlorobenzaldehyde → Methyl 4-((3-chlorobenzyl)amino)butanoate hydrochloride

HRID 408622
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인쇄 미리보기

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HRID 408622 반응식
Cl.[CH3:2][O:3][C:4](=[O:9])[CH2:5][CH2:6][CH2:7][NH2:8].[Cl:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=1)[CH:14]=O.[O-]S([O-])(=O)=O.[Mg+2].[BH4-].[Na+]>C1COCC1.CO>[ClH:10].[CH3:2][O:3][C:4](=[O:9])[CH2:5][CH2:6][CH2:7][NH:8][CH2:14][C:13]1[CH:16]=[CH:17][CH:18]=[C:11]([Cl:10])[CH:12]=1
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참가 물질

7

반응물 4

HCID 114773-ChlorobenzaldehydeHCID 24083Sulfuric acid magnesium salt (1:1)HCID 27563834-Aminobutyric acid methyl ester hydrochlorideHCID 4311764Sodium borohydride

생성물 1

HCID 70558726Methyl 4-((3-chlorobenzyl)amino)butanoate hydrochloride수율 65%

시약·촉매·용매 2

HCID 887
Methanol
용매
HCID 8028Tetrahydrofuran용매

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온도
20 °C

실험 절차

To a solution of 4-amino-butyric acid methyl ester hydrochloride (30 g, 1 eq.) in 360 mL of THF were added TEA (67.7 mL, 2.5 eq.), then 3-chlorobenzaldehyde (19 mL, 0.9 eq.) and MgSO4 (35 g, 1.5 eq.). The reaction was stirred at 20° C. for 15 h under nitrogen. 360 mL of MeOH was added then the reaction was cooled to −20° C. NaBH4 (14.75 g, 2 eq.) was added portionwise. The reaction was stirred for 1 h at 0° C. The crude was partially concentrated under reduced pressure at 20° C., filtered and washed with DCM. The filtrate was washed with water and brine. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure at 20° C. The residue, in solution in 1600 mL of Et2O, was treated with 87 mL of HCl 2N in Et2O. A solid was formed, filtrated, washed with Et2O, then pentane and dried to afford 4-(3-chloro-benzylamino)-butyric acid methyl ester hydrochloride (32 g, yield=65%).

후처리

  1. temperaturethe reaction was cooled to −20° C
  2. stirringThe reaction was stirred for 1 h at 0° C
  3. concentrationThe crude was partially concentrated under reduced pressure at 20° C.
  4. filtrationfiltered
  5. washwashed with DCM
  6. washThe filtrate was washed with water and brine
  7. dry with materialThe organic layer was dried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure at 20° C
  10. additionThe residue, in solution in 1600 mL of Et2O, was treated with 87 mL of HCl 2N in Et2O
  11. customA solid was formed
  12. filtrationfiltrated
  13. washwashed with Et2O
  14. dry with materialpentane and dried

출처 및 근거

ORD 기록
ord-8447e0516973421b80519cf907fa3dbe
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08759334B2

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