Hydrogen Bromide → 5-Bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine

HRID 1054446ノート

反応式

HRID 1054446 の反応式
N([O-])=O.[Na+].[F:5][C:6]1[CH:7]=[C:8](N)[C:9]2[O:14][CH2:13][CH2:12][O:11][C:10]=2[CH:15]=1.[BrH:17]>O>[Br:17][C:8]1[C:9]2[O:14][CH2:13][CH2:12][O:11][C:10]=2[CH:15]=[C:6]([F:5])[CH:7]=1

参加物

5

反応物 3

HCID 260Hydrogen Bromide2 回HCID 23668193Sodium NitriteHCID 666806007-Fluoro-2,3-dihydro-1,4-benzodioxin-5-amine

生成物 1

HCID 896359545-Bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

NaNO2 (2.69 g, 39.9 mmol) in water (20 mL) was added slowly at 0° C. to a solution of 7-fluoro-2,3-dihydrobenzo[b][1,4]dioxin-5-amine (4.5 g, 26 mmol) in aq. 47% HBr (20 mL) and continued stirring at same temperature for 30 min. The above diazonium salt solution was added slowly to a solution of CuBr (5.7 g, 39.9 mmol) in aq. 47% HBr (25 mL) at 0° C. and stirred at 25° C. for 30 min. Reaction mixture was quenched with ice water, extracted with ethyl acetate (3×50 mL), washed it with water followed by brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford crude. The crude was purified by column purification (using silica gel and 0-5% ethyl acetate in Hexane as eluent) to afford 5-bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine (Int-28) (5.9 g). 1H NMR (300 MHz, CDCl3) δ 6.9-6.84 (1H, dd), 6.6-6.5 (1H, dd), 4.3-4.3 (4H, m) ppm.

後処理

  1. stirringstirred at 25° C. for 30 min
  2. customReaction mixture
  3. customwas quenched with ice water
  4. extractionextracted with ethyl acetate (3×50 mL)
  5. washwashed it with water
  6. dry with materialdried over anhydrous sodium sulphate
  7. concentrationconcentrated under reduced pressure
  8. customto afford crude
  9. customThe crude was purified by column purification (using silica gel and 0-5% ethyl acetate in Hexane as eluent)

出典と根拠

ORDレコード
ord-cdfa4b24b41041958c6c4102f335dc2f
出典データセット
uspto-grants-2016_07
特許番号
US09394305B2

反応ノート

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