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Water → 5-Amino-2-(3,3,3-trifluoropropyl)benzofuran

HRID 582619
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HRID 582619 반응식
[F:1][C:2]([F:18])([F:17])[CH2:3][CH2:4][C:5]1[O:6][C:7]2[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[CH:10][C:8]=2[CH:9]=1.[BH4-].[Na+].O>CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)C.[Cl-].[Pd].ClCCl>[NH2:14][C:11]1[CH:12]=[CH:13][C:7]2[O:6][C:5]([CH2:4][CH2:3][C:2]([F:18])([F:1])[F:17])=[CH:9][C:8]=2[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 22132946HCID 22132946, 화합물

생성물 1

HCID 221329575-Amino-2-(3,3,3-trifluoropropyl)benzofuran

시약·촉매·용매 3

HCID 21218Trioctylmethylammonium chloride촉매HCID 23938Palladium촉매
HCID 6344
Dichloromethane
용매

실험 절차

A mixture of 2.4 g (9.2 mmol) of 2-(3,3,3-trifluoropropyl)-5-nitrobenzofuran, 0.65 g (17 mmol) of sodium borohydride, 45 mg of Adogen 464 and 0.38 g of 10% palladium on carbon containing 50% of water is stirred for 5 hours in 95 ml of dichloromethane and 48 ml of water, then it is filtered on silica and the silica is rinsed with ethanol. The filtrate is then concentrated under reduced pressure and coevaporated with toluene. After chromatography of the residue on a silica column using a 0-30% mixture of ethyl acetate in cyclohexane, 2.0 g of product are obtained.

후처리

  1. filtration48 ml of water, then it is filtered on silica
  2. washthe silica is rinsed with ethanol
  3. concentrationThe filtrate is then concentrated under reduced pressure
  4. customare obtained

출처 및 근거

ORD 기록
ord-f0da99b1290046519b91d429c421e01a
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05925662

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