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Trifluoroacetic acid → 4-[2-(3-Chloropropylamino)ethyl]benzonitrile trifluoroacetate

HRID 1591758
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HRID 1591758 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][N:5]([CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]#[N:22])=[CH:17][CH:16]=1)C(=O)OC(C)(C)C.[F:23][C:24]([F:29])([F:28])[C:25]([OH:27])=[O:26]>ClCCl>[F:23][C:24]([F:29])([F:28])[C:25]([OH:27])=[O:26].[Cl:1][CH2:2][CH2:3][CH2:4][NH:5][CH2:13][CH2:14][C:15]1[CH:16]=[CH:17][C:18]([C:21]#[N:22])=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 58638721tert.-Butyl (3-chloropropyl)-[2-(4-cyanophenyl)ethyl]carbamate

생성물 1

HCID 693492044-[2-(3-Chloropropylamino)ethyl]benzonitrile trifluoroacetate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 626 mg (1.94 mmol) of tert.-butyl (3-chloropropyl)-[2-(4-cyanophenyl)ethyl]carbamate and 5.0 ml of trifluoroacetic acid in 20 ml of dichloromethane was stirred at room temperature for 1.5 hours and then evaporated to dryness. The residue was triturated with diethyl ether. The precipitate formed was then filtered off and dried under reduced pressure over calcium chloride. The product obtained in this manner was reacted further without additional purification.

후처리

  1. customevaporated to dryness
  2. customThe residue was triturated with diethyl ether
  3. customThe precipitate formed
  4. filtrationwas then filtered off
  5. dry with materialdried under reduced pressure over calcium chloride
  6. customThe product obtained in this manner
  7. customwas reacted further without additional purification

출처 및 근거

ORD 기록
ord-ce3aba9652a64e66ac7637fce09d1c71
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07291642B2

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