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Iodine → HCID 68283768, 화합물

HRID 1527446
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HRID 1527446 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][C:9]([F:12])([F:11])[F:10].[Li]CCCC.CN(CCN(C)C)C.[I:26]I>C1COCC1>[F:1][C:2]1[C:3]([O:8][C:9]([F:11])([F:10])[F:12])=[CH:4][CH:5]=[CH:6][C:7]=1[I:26]
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참가 물질

6

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HCID 807IodineHCID 8037N,N,N',N'-TetramethylethylenediamineHCID 27772832-(Trifluoromethoxy)fluorobenzeneHCID 178418339Butyllithium

생성물 1

HCID 68283768HCID 68283768, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
-78 °C

실험 절차

To a solution of 1-fluoro-2-(trifluoromethoxy)benzene [2106-18-5] (20.0 g, 111 mmol) in dry THF (200 mL), cooled to −78° C., was added dropwise n-BuLi (2.5 M solution in n-hexane; 65 mL, 160 mmol) and subsequently TMEDA (60 mL). The reaction mixture was stirred for additional 60 min at −78° C., followed by addition of a solution of iodine (30.2 g, 120 mmol) in dry THF (50 mL). The resulting mixture was stirred for 1 h and then quenched by addition of a saturated aqueous NH4Cl solution (20 mL). The organic layer was washed with 1N HCl, water and brine, and dried over MgSO4. Volatiles were removed in vacuo to afford the title compound as yellow oil. The product was used in the next reaction step without further purification. MS (LC/MS): 306.0 [M+H]+.

후처리

  1. stirringThe resulting mixture was stirred for 1 h
  2. customquenched by addition of a saturated aqueous NH4Cl solution (20 mL)
  3. washThe organic layer was washed with 1N HCl, water and brine
  4. dry with materialdried over MgSO4
  5. customVolatiles were removed in vacuo

출처 및 근거

ORD 기록
ord-e87bba9db86347c29192296e23d8e613
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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