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2-Amino-6-(trifluoromethyl)benzoic acid → HCID 54486842, 화합물

HRID 1056441
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HRID 1056441 반응식
[NH2:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[C:3]=1[C:4](O)=[O:5].[H-].[H-].[H-].[H-].[Li+].[Al+3]>O1CCCC1>[NH2:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:12])([F:13])[F:14])[C:3]=1[CH2:4][OH:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 27785082-Amino-6-(trifluoromethyl)benzoic acidHCID 21226445Aluminium lithium hydride2회

생성물 1

HCID 54486842HCID 54486842, 화합물수율 97%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

2-amino-6-(trifluoromethyl)benzoic acid (20 g, 97 mmol) was dissolved in tetrahydrofuran (120 mL) in a 3-neck RB flask equipped with an addition funnel and a condenser. The solution was cooled in an ice-water bath. LiAlH4 (83 mL, 166 mmol) (2M solution in THF) was then added dropwise. After all of the LiAlH4 solution was added, the reaction mixture was allowed to warm to room temperature and stirred at room temperature overnight. The reaction was then quenched by adding 10 mL of Water, then 10 mL of 15% NaOH and then 25 mL of Water. The salts were filtered off and the solvents were evaporated under vacuum. The product was used as is (18 g, 97% yield.

후처리

  1. customequipped with an addition funnel and a condenser
  2. temperatureThe solution was cooled in an ice-water bath
  3. customThe reaction was then quenched
  4. additionby adding 10 mL of Water
  5. filtrationThe salts were filtered off
  6. customthe solvents were evaporated under vacuum

출처 및 근거

ORD 기록
ord-d2c9abc313334f12b8b680d62f767f92
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09397302B2

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