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Tetrabutylammonium Fluoride → 2-(2-Ethynylphenyl)propanamide

HRID 592357
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HRID 592357 반응식
CCCC[N+](CCCC)(CCCC)CCCC.[F-].C[Si]([C:23]#[C:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[CH:31]([CH3:35])[C:32]([NH2:34])=[O:33])(C)C>C1COCC1.C([O-])(O)=O.[Na+]>[C:24]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[CH:31]([CH3:35])[C:32]([NH2:34])=[O:33])#[CH:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 867122802-(2-((Trimethylsilyl)ethynyl)phenyl)propanamide

생성물 1

HCID 867122792-(2-Ethynylphenyl)propanamide

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회HCID 516892Sodium Bicarbonate용매

실험 절차

A 1.0 M solution of TBAF in THF (45.6 mL, 45.6 mmol) was added to a solution of 2-(2-((trimethylsilyl)ethynyl)phenyl)propanamide I15 (9.33 g, 38.0 mmol) in THF (200 mL) and the mixture was stirred for 10 minutes. The reaction mixture was diluted with sat. aq. NaHCO3 (200 mL), and the aqueous layer was extracted with DCM (3×150 mL). The combined organics were adsorbed onto silica and purified by silica gel column chromatography (Biotage Isolera, 120 g SiO2 cartridge, 0-80% EtOAc in petroleum benzine 40-60° C.) to yield the title compound K7 as a tan solid (5.11 g, 76%). LCMS-D: rt 3.03 min; m/z 174 [M+H]+.

후처리

  1. extractionthe aqueous layer was extracted with DCM (3×150 mL)
  2. custompurified by silica gel column chromatography (Biotage Isolera, 120 g SiO2 cartridge, 0-80% EtOAc in petroleum benzine 40-60° C.)

출처 및 근거

ORD 기록
ord-f73f952dec364400a637c6ece9b71df1
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238644B2

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