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Iodine → HCID 68283768、化合物

HRID 1527446
ノート
印刷プレビュー

反応式

HRID 1527446 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

HCID 68283768HCID 68283768、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

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]+.

後処理

  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

出典と根拠

ORDレコード
ord-e87bba9db86347c29192296e23d8e613
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09085555B2

反応ノート

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