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Hydrochloric Acid → 4-(2-Benzyloxy-4-ethylphenoxy)-3-fluoroaniline

HRID 626035
ノート
印刷プレビュー

反応式

HRID 626035 の反応式
[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([CH2:15][CH3:16])[CH:12]=[CH:11][C:10]=1[O:17][C:18]1[CH:23]=[CH:22][C:21]([N+:24]([O-])=O)=[CH:20][C:19]=1[F:27])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Sn](Cl)Cl.Cl.[OH-].[Na+]>CCOCC>[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([CH2:15][CH3:16])[CH:12]=[CH:11][C:10]=1[O:17][C:18]1[CH:23]=[CH:22][C:21]([NH2:24])=[CH:20][C:19]=1[F:27])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物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 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 24479Stannous ChlorideHCID 591912382-(Benzyloxy)-4-ethyl-1-(2-fluoro-4-nitrophenoxy)benzene

生成物 1

HCID 591912224-(2-Benzyloxy-4-ethylphenoxy)-3-fluoroaniline収率 68.9%

試薬・触媒・溶媒 1

HCID 3283
Diethyl Ether
溶媒

実験手順

To a solution of 2-(benzyloxy)-4-ethyl-1-(2-fluoro-4-nitro phenoxy)benzene (25 g; 68 mmol) in ether (86 mL), under argon cooled to 0° C., was added a suspension of tin dichloride (153 g; 801 mmol) in HCl (50 mL; 2 mol). The mixture was allowed to warm up to room temperature overnight, then a 10% NaOH solution was added dropwise. The resulting mixture was extracted with ethyl acetate (5*400 mL). Combined organic phases were washed with water (400 mL) and brine, then dried over Na2SO4 and concentrated. The residue was purified on silica gel (ethyl acetate/cyclohexane 1:9) to yield the title compound as a light brown solid (15.8 g; 68.8%)

後処理

  1. additionwas added
  2. extractionThe resulting mixture was extracted with ethyl acetate (5*400 mL)
  3. washCombined organic phases were washed with water (400 mL) and brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. customThe residue was purified on silica gel (ethyl acetate/cyclohexane 1:9)

出典と根拠

ORDレコード
ord-8a3960b2a6a64f0e8ec1507a97a59043
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309179B2

反応ノート

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