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Dimethylformamide → 4-Ethylthiophene-3-carboxaldehyde

HRID 1290242
ノート
印刷プレビュー

反応式

HRID 1290242 の反応式
Br[C:2]1[C:6]([CH2:7][CH3:8])=[CH:5][S:4][CH:3]=1.[Li]CCCC.CN([CH:17]=[O:18])C>C(OCC)C>[CH2:7]([C:6]1[C:2]([CH:17]=[O:18])=[CH:3][S:4][CH:5]=1)[CH3:8]
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

5

反応物 3

HCID 6228DimethylformamideHCID 1279238983663-39-2HCID 178418339Butyllithium

生成物 1

HCID 189238504-Ethylthiophene-3-carboxaldehyde

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
-20 °C

実験手順

A solution of 3-bromo-4-ethylthiophene, B9, (3.4 g, 0.018 mol) in 40 mL of diethyl ether was cooled to -78° C., and a solution of n-BuLi (12.0 mL, 1.6M) in hexanes was added dropwise. The solution was allowed to warm to -20° C., and DMF (1.46 g, 0.020 mol) was added. The reaction mixture was allowed to warm to ambient temperature and was stirred overnight. The reaction was quenched with aqueous ammonium chloride solution and extracted twice with diethyl ether. The organic extracts were combined, washed with twice with water and then brine and dried (MgSO4). The solution was filtered and concentrated to provide 4-ethylthiophene-3-carboxaldehyde, C9, which was used directly in the next step. ##STR65##

後処理

  1. temperatureto warm to ambient temperature
  2. customThe reaction was quenched with aqueous ammonium chloride solution
  3. extractionextracted twice with diethyl ether
  4. washwashed with twice with water
  5. dry with materialbrine and dried (MgSO4)
  6. filtrationThe solution was filtered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-01f371808dbf4eadbd6df805f21b0e69
出典データセット
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05750720

反応ノート

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