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Hydrochloric Acid → HCID 14052568, 화합물

HRID 330076
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HRID 330076 반응식
Br[C:2]1[C:3]([F:11])=[C:4]([CH3:10])[C:5]([F:9])=[C:6]([F:8])[CH:7]=1.Cl.[CH3:13][N:14]1CCCC1=O>O>[F:11][C:3]1[C:4]([CH3:10])=[C:5]([F:9])[C:6]([F:8])=[CH:7][C:2]=1[C:13]#[N:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 13387N-methyl-2-pyrrolidoneHCID 140525671-Bromo-2,4,5-trifluoro-3-methylbenzene

생성물 1

HCID 14052568HCID 14052568, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 3-bromo-2,5,6-trifluorotoluene (11.0 g) and cupric cyanide (5.3 g) in N-methylpyrrolidone (15 ml) was stirred at 150° to 160° C. in a sealed tube for 4.5 hours. After cooling, to the reacting mixture was added a solution of ferric chloride (20 g) and concentrated hydrochloric acid (5 ml) in water (30 ml) and stirred at 50° to 60° C. for 20 minutes. The reacting mixture was extracted with ether, the organic layer was washed with aqueous hydrochloric acid solution, water and saturated aqueous sodium chloride solution successively, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound (7.83 g) as pale brown oil.

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후처리

  1. temperatureAfter cooling, to the reacting mixture
  2. stirringstirred at 50° to 60° C. for 20 minutes
  3. extractionThe reacting mixture was extracted with ether
  4. washthe organic layer was washed with aqueous hydrochloric acid solution, water and saturated aqueous sodium chloride solution successively
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3400fbc7f7404634af49de6bfc2a5e4a
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04894458

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