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Water → Methyl 2-amino-4-(2-chloroethoxy)-5-methoxybenzoate

HRID 612031
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HRID 612031 반응식
[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([O:10][CH3:11])[C:7]([O:12][CH2:13][CH2:14][Cl:15])=[CH:6][C:5]=1[N+:16]([O-])=O.[Cl-].[NH4+].O>[Fe].CO>[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([O:10][CH3:11])[C:7]([O:12][CH2:13][CH2:14][Cl:15])=[CH:6][C:5]=1[NH2:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 23032998Methyl 4-(2-chloroethoxy)-5-methoxy-2-nitrobenzoate

생성물 1

HCID 23033001Methyl 2-amino-4-(2-chloroethoxy)-5-methoxybenzoate

시약·촉매·용매 2

HCID 23925Iron촉매HCID 887Methanol용매

실험 절차

A mixture of 68.2 g (235.4 mmol) of 4-(2-chloro-ethoxy)-5-methoxy-2-nitro-benzoic acid methyl ester and 52.6 g (941.8 mmol) of iron was mechanically stirred at reflux in a mixture containing 62.9 g ammonium chloride, 393 ml water, and 1021 ml methanol for 15 hr. The mixture was concentrated and mixed with ethyl acetate. The organic solution was washed with water and saturated sodium bicarbonate. The solution was dried over magnesium sulfate and filtered through a short column of silica gel. The solution was concentrated to 200 ml and diluted with 250 of hot hexane. After standing 47.7 g of the tide compound was obtained as a solid: mass spectrum (electrospray, m/e) M+H 259.8.

후처리

  1. temperatureat reflux in a mixture
  2. concentrationThe mixture was concentrated
  3. additionmixed with ethyl acetate
  4. washThe organic solution was washed with water and saturated sodium bicarbonate
  5. dry with materialThe solution was dried over magnesium sulfate
  6. filtrationfiltered through a short column of silica gel
  7. concentrationThe solution was concentrated to 200 ml
  8. additiondiluted with 250 of hot hexane
  9. customwas obtained as a solid

출처 및 근거

ORD 기록
ord-1942ddee23b8431584402a4677f4fea8
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06002008

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