Benzene, 1-bromo-3,5-dimethyl- → (3,5-dimethylphenyl)(2-methylcyclopropyl)Methanone

HRID 1292402

반응식

HRID 1292402 반응식
Br[C:2]1[CH:3]=[C:4]([CH3:9])[CH:5]=[C:6]([CH3:8])[CH:7]=1.C([Li])CCC.CON(C)[C:18]([CH:20]1[CH2:22][CH:21]1[CH3:23])=[O:19]>CCCCCC>[CH3:9][C:4]1[CH:3]=[C:2]([C:18]([CH:20]2[CH2:22][CH:21]2[CH3:23])=[O:19])[CH:7]=[C:6]([CH3:8])[CH:5]=1

참가 물질

5

반응물 3

HCID 136357Benzene, 1-bromo-3,5-dimethyl-HCID 45084206N-methoxy-N,2-dimethylcyclopropane-1-carboxamideHCID 178418339Butyllithium

생성물 1

HCID 21249913(3,5-dimethylphenyl)(2-methylcyclopropyl)Methanone

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

To a solution of 5-bromo-meta-xylene (5.7 mL in 120 mL of dry tetrahydrofuran) at -78° C. was added 30.6 mL of a 1.4M solution of n-butyllithium in hexane and the mixture stirred at low temperature. After 15 minutes, a solution of 2-methylcyclopropanecarboxylic acid N-methoxy-N-methyl-amide (5.0 g in 50 mL tetrahydrofuran) was added dropwise over 5 minutes and the mixture then allowed to warm slowly to room temperature. After 1 hour, the reaction was quenched by the addition of 20 mL 2N hydrochloric acid and 40 mL water. This was extracted with ethyl acetate washed with saturated sodium bicarbonate and brine then dried over sodium sulfate to give 6.95 g of the crude title compound.

후처리

  1. waitAfter 1 hour
  2. customthe reaction was quenched by the addition of 20 mL 2N hydrochloric acid and 40 mL water
  3. extractionThis was extracted with ethyl acetate
  4. washwashed with saturated sodium bicarbonate and brine
  5. dry with materialthen dried over sodium sulfate

출처 및 근거

ORD 기록
ord-8885e1a9a59b4a849dcb053263a64fbf
출처 데이터셋
uspto-grants-1998_05
특허 번호
US05756507

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