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Dimethylformamide → 2-Azido-1-(4-methylsulfanyl-phenyl)-ethanone

HRID 1908252
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HRID 1908252 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([S:11][CH3:12])=[CH:7][CH:6]=1)=[O:4].CN(C=O)C.[N-:18]=[N+:19]=[N-:20].[Na+]>CCOC(C)=O>[N:18]([CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([S:11][CH3:12])=[CH:7][CH:6]=1)=[O:4])=[N+:19]=[N-:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 33557Sodium AzideHCID 27375232-Bromo-1-(4-methylsulfanylphenyl)ethanone

생성물 1

HCID 161273432-Azido-1-(4-methylsulfanyl-phenyl)-ethanone수율 100%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
15 °C
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실험 절차

A solution consisting of 2-bromo-1-(4-methylsulfanyl-phenyl)-ethanone (2.00 g, 8.16 mmol) and DMF (7 mL) was cooled to 15° C. and treated portion-wise with sodium azide (583 mg, 8.98 mmol). Once addition was complete, the reaction mixture was stirred for 3 h with gradual warming to rt. The reaction mixture was then diluted with EtOAc (20 mL) and washed with water (25 mL×2), NaHCO3 (satd., 25 mL×2), and brine. The combined organic phases were dried (Na2SO4) and concentrated to dryness to yield the title compound (1.69 g, 100%).

후처리

  1. additionOnce addition
  2. temperaturewith gradual warming to rt
  3. washwashed with water (25 mL×2), NaHCO3 (satd., 25 mL×2), and brine
  4. dry with materialThe combined organic phases were dried (Na2SO4)
  5. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-6bbde4efda324d1bb92722c4b543e8d2
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08598202B2

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