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4-Azidomethyl-2-(2-methylphenyl)benzoic acid methyl ester → 4-Aminomethyl-2-(2-methylphenyl)benzoic acid methyl ester

HRID 383161
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반응식

HRID 383161 반응식
[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]=[N+]=[N-])=[CH:6][C:5]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH3:20]>CO.Cl>[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][NH2:11])=[CH:6][C:5]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 206998904-Azidomethyl-2-(2-methylphenyl)benzoic acid methyl ester

생성물 1

HCID 206998884-Aminomethyl-2-(2-methylphenyl)benzoic acid methyl ester수율 30.1%

시약·촉매·용매 2

HCID 313Hydrochloric Acid촉매HCID 887Methanol용매

실험 절차

To a flask at ambient temperature under N2 containing 10% palladium on carbon catalyst (1.0 g) was added a solution of 4-azidomethyl-2-(2-methylphenyl)benzoic acid methyl ester (5.00 g, 17.8 mmol), prepared as in Example 1191A, in MeOH (75 mL). Two drops of conc. HCl added, and reaction stirred vigorously overnight under an atmosphere of H2. Catalyst filtered off through celite and washed with MeOH. Filtrate concentrated in vacuo, and residue taken up in an aqueous 4N NaOH solution. Aqueous solution extracted with CHCl3 (3×), and extracts dried with Na2SO4, filtered, and concentrated in vacuo to afford the desired product (1.37 g, 30%). m/e (DCI) 256 (MH+)

후처리

  1. additionTo a flask at ambient temperature under N2 containing 10% palladium on carbon catalyst (1.0 g) was added
  2. customreaction
  3. filtrationCatalyst filtered off through celite
  4. washwashed with MeOH
  5. concentrationFiltrate concentrated in vacuo, and residue
  6. extractionAqueous solution extracted with CHCl3 (3×), and extracts
  7. dry with materialdried with Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0f8b198dd3d34025bdbea41c1ea81023
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06310095B1

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