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Water → 4-Amino-5-cyano-2-hydroxy-3-methylbenzoic acid

HRID 1443448
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HRID 1443448 반응식
[Li+].[OH-].O.C([O:6][C:7](=[O:19])[C:8]1[CH:13]=[C:12]([C:14]#[N:15])[C:11]([NH2:16])=[C:10]([CH3:17])[C:9]=1[OH:18])C>C(O)C.O>[NH2:16][C:11]1[C:12]([C:14]#[N:15])=[CH:13][C:8]([C:7]([OH:19])=[O:6])=[C:9]([OH:18])[C:10]=1[CH3:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 2775029Ethyl 4-amino-5-cyano-2-hydroxy-3-methylbenzoate

생성물 1

HCID 125651984-Amino-5-cyano-2-hydroxy-3-methylbenzoic acid수율 98.9%

시약·촉매·용매 1

HCID 19096565Water ethanol용매

반응 조건

온도
80 °C

실험 절차

To a solution of LiOH×H2O (8.4 g, 0.2 mol) in ethanol/water (1:1, 300 mL) was added compound 74 (22 g, 0.1 mol) at RT and the reaction mixture was refluxed at 80° C. for 4 h. The reaction mixture was concentrated under vacuum, the obtained residue was diluted with water (100 mL), washed with pet. ether/ethyl acetate (1:1, 2×200 mL). The aqueous layer was separated, acidified to pH=5 using 1.5N HCl and the obtained solid product was filtered off. The aqueous layer was further extracted with ethyl acetate (2×300 mL), dried and concentrated to give more product. The combined products was washed with 5% ethyl acetate in pet. ether to give the pure title compound (19 g, >95%).

후처리

  1. concentrationThe reaction mixture was concentrated under vacuum
  2. additionthe obtained residue was diluted with water (100 mL)
  3. washwashed with pet. ether/ethyl acetate (1:1, 2×200 mL)
  4. customThe aqueous layer was separated
  5. filtrationthe obtained solid product was filtered off
  6. extractionThe aqueous layer was further extracted with ethyl acetate (2×300 mL)
  7. customdried
  8. concentrationconcentrated
  9. customto give more product
  10. washThe combined products was washed with 5% ethyl acetate in pet. ether

출처 및 근거

ORD 기록
ord-ae4b9b919db04ec7a0d59ca0b4ff3a8d
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07659245B2

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