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N-methoxy-N-methyl-4-(pentafluoro-lambda6-sulfanyl)benzamide → 1-[4-(Pentafluoro-lambda6-sulfanyl)phenyl]ethan-1-one

HRID 1523309
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HRID 1523309 반응식
CON(C)[C:4](=[O:17])[C:5]1[CH:10]=[CH:9][C:8]([S:11]([F:16])([F:15])([F:14])([F:13])[F:12])=[CH:7][CH:6]=1.[CH3:19][Li]>C1COCC1>[F:12][S:11]([F:16])([F:15])([F:14])([F:13])[C:8]1[CH:9]=[CH:10][C:5]([C:4](=[O:17])[CH3:19])=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 58360637N-methoxy-N-methyl-4-(pentafluoro-lambda6-sulfanyl)benzamideHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 597155361-[4-(Pentafluoro-lambda6-sulfanyl)phenyl]ethan-1-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a solution of N-methoxy-N-methyl-4-(pentafluoro-λ6-sulfanyl)benzamide (Preparation 42, 3.0 g, 10.3 mmol) in THF (100 mL) at 0° C. was added drop-wise methyl lithium (1.5M solution, 10.3 mL, 15.5 mmol). The reaction was stirred at 0° C. for 2 hours, then quenched with a saturated aqueous solution of ammonium acetate. The reaction was extracted with ethyl acetate and dried over MgSO4 before concentrating in vacuo to afford the title compound that was used without further purification.

후처리

  1. customquenched with a saturated aqueous solution of ammonium acetate
  2. extractionThe reaction was extracted with ethyl acetate
  3. dry with materialdried over MgSO4
  4. concentrationbefore concentrating in vacuo

출처 및 근거

ORD 기록
ord-0c2e418a45504bc3aba04b33a229415d
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09079878B2

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