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2-Bromo-4'-(trifluoromethyl)acetophenone → 2-Thiocyanato-1-(4-trifluoromethyl-phenyl)-ethanone

HRID 1667661
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인쇄 미리보기

반응식

HRID 1667661 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:7][CH:6]=1)=[O:4].[S-:15][C:16]#[N:17].[K+]>C(O)C>[S:15]([CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]([F:14])([F:13])[F:12])=[CH:7][CH:6]=1)=[O:4])[C:16]#[N:17]
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참가 물질

4

반응물 2

HCID 3219792-Bromo-4'-(trifluoromethyl)acetophenoneHCID 516872Potassium thiocyanate

생성물 1

HCID 575420642-Thiocyanato-1-(4-trifluoromethyl-phenyl)-ethanone수율 95.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 25.64 g (96.0 mmole) of 2-bromo-1-(4-trifluoromethyl-phenyl)-ethanone, 10.27 g (105.7 mmole) of potassium thiocyanate and 130 mL of ethanol (130 mL) was heated to reflux for 2 hours, and then concentrated under reduced pressure. The residue was taken up in 700 mL of ethyl acetate, washed three times with 75 mL of water, then 75 mL of brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 22.57 g of 2-thiocyanato-1-(4-trifluoromethyl-phenyl)-ethanone as an orange-brown solid.

후처리

  1. temperatureto reflux for 2 hours
  2. concentrationconcentrated under reduced pressure
  3. washwashed three times with 75 mL of water
  4. dry with material75 mL of brine, dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-275a5f4ff45846299b617230ce112ff2
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044213B2

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