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Sodium borohydride → 5-Amino-2-(3,3,3-trifluoropropyl)benzofuran

HRID 1856816
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HRID 1856816 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+]>[Pd].ClCCl.O>[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
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참가 물질

6

반응물 2

HCID 4311764Sodium borohydrideHCID 22132946HCID 22132946, 화합물

생성물 1

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

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 962Water용매2회HCID 6344Dichloromethane용매

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 (methyl trialkylammonium chloride) and 0.38 g of 5% palladium on carbon containing 50% of water in 95 ml of dichloromethane and 48 ml of water is stirred for 5 hours, 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. By 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. Melting point: 74° C.

후처리

  1. filtrationit 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-1c3910b4c00042bc9275efe2f3d697e3
출처 데이터셋
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06143772

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