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Trifluoroacetic acid → 2-(2-Aminoethyl)-4-bromophenyl benzyl ether

HRID 1106844
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인쇄 미리보기

반응식

HRID 1106844 반응식
[BH4-].[Na+].FC(F)(F)C(O)=O.[CH2:10]([O:17][C:18]1[CH:23]=[CH:22][C:21]([Br:24])=[CH:20][C:19]=1[CH2:25][C:26]#[N:27])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C1COCC1>[CH2:10]([O:17][C:18]1[CH:23]=[CH:22][C:21]([Br:24])=[CH:20][C:19]=1[CH2:25][CH2:26][NH2:27])[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 4311764Sodium borohydrideHCID 226754674-Bromo-2-cyanomethylphenyl benzyl ether

생성물 1

HCID 179382632-(2-Aminoethyl)-4-bromophenyl benzyl ether수율 108.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a mixture of NaBH4 (6.0 g) in THF (100 ml) was added dropwise trifluoroacetic acid (18 ml) at 0° C. (ice bath). 4-Bromo-2-cyanomethylphenyl benzyl ether (10 g) was added and the mixture stirred at ambient temperature for 18 hours. The reaction was quenched with water (100 ml), the pH adjusted to 13 with 2N aqueous NaOH solution, and extracted with diethyl ether. The diethyl ether extracts were dried (MgSO4) and evaporated to give 2-(2-aminoethyl)-4-bromophenyl benzyl ether (11.0 g) as a yellow gum,

후처리

  1. customThe reaction was quenched with water (100 ml)
  2. extractionextracted with diethyl ether
  3. dry with materialThe diethyl ether extracts were dried (MgSO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-a6ebd848c30847d0ae91d9c799703076
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06057345

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