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Methyl 2,4-dimethyl-3-nitrobenzoate → Methyl 3-amino-2,4-dimethylbenzoate

HRID 1427075
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HRID 1427075 반응식
[CH3:1][C:2]1[C:11]([N+:12]([O-])=O)=[C:10]([CH3:15])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]>CO.[Pd]>[NH2:12][C:11]1[C:2]([CH3:1])=[C:3]([CH:8]=[CH:9][C:10]=1[CH3:15])[C:4]([O:6][CH3:7])=[O:5]
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참가 물질

4

반응물 1

HCID 71744216Methyl 2,4-dimethyl-3-nitrobenzoate

생성물 1

HCID 66871802Methyl 3-amino-2,4-dimethylbenzoate수율 65%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of methyl 2,4-dimethyl-3-nitro-benzoate (37 g, 176.9 mmol) in methanol (370 mL), 10% palladium on carbon 50% wet (5.6 g) is added. The reaction is bubbled with hydrogen and placed under a hydrogen atmosphere for 6 days. The mixture is filtered through diatomaceous earth and the filtrate is evaporated to dryness. The resulting residue is purified by flash chromatography (silica gel), eluting with 20% ethyl acetate in hexanes to afford the title compound as a yellow oil (20.5 g, 65%). Mass spectrum (m/z): 180.1 (M+1). 1H NMR (300.16 MHz, DMSO-d6): δ 6.89 (s, 2H), 4.78 (s, 2H), 3.76 (s, 3H), 2.23 (s, 3H), 2.12 (s, 3H).

후처리

  1. customThe reaction is bubbled with hydrogen
  2. filtrationThe mixture is filtered through diatomaceous earth
  3. customthe filtrate is evaporated to dryness
  4. customThe resulting residue is purified by flash chromatography (silica gel)
  5. washeluting with 20% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-ac654275b62d4456b909d4c8b6dd18d9
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08933098B2

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