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Diisobutylaluminum hydride → HCID 67233948、化合物

HRID 1041975
ノート
印刷プレビュー

反応式

HRID 1041975 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([F:17])[CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:12](OCC)=[O:13])[CH:8]=[CH:7]2.CC(C[AlH]CC(C)C)C>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([F:17])[CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([CH2:12][OH:13])[CH:8]=[CH:7]2
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

4

反応物 2

HCID 14487Diisobutylaluminum hydrideHCID 67234511HCID 67234511、化合物

生成物 1

HCID 67233948HCID 67233948、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

Ethyl 8-bromo-6-fluoroquinoline-2-carboxylate (3.201 g, 10.7 mmol) was weighed into a flask, and dissolved in 100 mL of DCM. The reaction was cooled to −78° C., followed by drop-wise addition of DIBAL-H (21.48 mL, 32.22 mmol) over 10 minutes. The reaction was then allowed to stir and warm to ambient temperature over 2 hours at which time the starting material had been consumed. The reaction was quenched with 10 mL MeOH, followed by addition of 100 mL of Rochelle's Salts, and stirred overnight to remove the emulsion. The reaction was then partitioned with ethyl acetate. The combined organic fractions were concentrated in vacuo. The crude semi solid was purified by flash column chromatography (eluting with a 20-50% ethyl acetate/hexanes gradient), affording the desired product as an orange-yellow semi solid (2.27 g, 42% yield) MS APCI (+) m/z 256.1 and 258 (M+1 of each Br isotope) detected.

後処理

  1. temperaturewarm to ambient temperature over 2 hours at which time the starting material
  2. customhad been consumed
  3. customThe reaction was quenched with 10 mL MeOH
  4. additionfollowed by addition of 100 mL of Rochelle's Salts
  5. stirringstirred overnight
  6. customto remove the emulsion
  7. customThe reaction was then partitioned with ethyl acetate
  8. concentrationThe combined organic fractions were concentrated in vacuo
  9. customThe crude semi solid was purified by flash column chromatography (
  10. washeluting with a 20-50% ethyl acetate/hexanes gradient),

出典と根拠

ORDレコード
ord-57c22734503f48a6a9a891278dd8452b
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08557809B2

反応ノート

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