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Ammonium thiocyanate → HCID 117833541, 화합물

HRID 1048627
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HRID 1048627 반응식
[F:1][C:2]1[C:7]([F:8])=[C:6]([F:9])[C:5]([F:10])=[C:4]([F:11])[C:3]=1[C:12](=[O:15])[CH2:13]Br.[S-:16][C:17]#[N:18].[NH4+].C(=O)(O)[O-].[Na+]>C(#N)C>[F:1][C:2]1[C:7]([F:8])=[C:6]([F:9])[C:5]([F:10])=[C:4]([F:11])[C:3]=1[C:12](=[O:15])[CH2:13][S:16][C:17]#[N:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 15666Ammonium thiocyanateHCID 516892Sodium BicarbonateHCID 27759632-Bromo-1-(pentafluorophenyl)ethan-1-one

생성물 1

HCID 117833541HCID 117833541, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
25 °C

실험 절차

A mixture of 1-(2,3,4,5,6-pentafluorophenyl)-2-bromo-1-ethanone 5.00 g, ammonium thiocyanate 1.58 g and acetonitrile 100 mL was stirred at 25° C. for one hour. To the reaction mixtures was added aqueous saturated sodium bicarbonate solution and the mixtures were extracted with ethyl acetate. The organic layers were washed with aqueous saturated sodium bicarbonate solution and were dried over anhydrous sodium sulfate. The resulting mixtures were concentrated under reduced pressure to give 1-(2,3,4,5,6-pentafluorophenyl)-2-thiocyanato-1-ethanone.

후처리

  1. customTo the reaction mixtures
  2. extractionthe mixtures were extracted with ethyl acetate
  3. washThe organic layers were washed with aqueous saturated sodium bicarbonate solution
  4. dry with materialwere dried over anhydrous sodium sulfate
  5. concentrationThe resulting mixtures were concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ebe6b4479277463cbb3ea1e6aa207453
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09380782B2

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