Hydrochloric Acid → 5-(Methoxymethyl)thiophene-2-carbaldehyde

HRID 629165ノート

反応式

HRID 629165 の反応式
Br[C:2]1[S:3][C:4]([CH2:7][O:8][CH3:9])=[CH:5][CH:6]=1.C([Li])CCC.CN(C)[CH:17]=[O:18].Cl>O1CCCC1.CN(C)P(N(C)C)(N(C)C)=O>[CH3:9][O:8][CH2:7][C:4]1[S:3][C:2]([CH:17]=[O:18])=[CH:6][CH:5]=1

参加物

6

反応条件

温度
-78 °C

実験手順

To a solution of 2-bromo-5-(methoxymethyl)thiophene (439 mg, 2.12 mmol) in 6 mL of 9:1 tetrahydrofuran/hexamethylphosphoramide under argon at −78° C. was added n-butyllithium (0.93 mL, 2.5 M in hexanes) dropwise. After stirring for 2 minutes at −78° C., dimethylformamide (0.82 mL, 10.6 mmol) was added in a single portion and the reaction mixture was allowed to warm to room temperature before being poured into 30 mL of 1 N hydrochloric acid. Organics were extracted with 1:1 ether/hexanes (3×30 mL), washed with water (2×30 mL, brine (30 mL), dried over magnesium sulfate, filtered and concentrated. The crude residue was subjected to chromatography on silica gel with gradient elution (5-20% ethyl acetate in hexanes) to give 5-(methoxymethyl)thiophene-2-carbaldehyde (103 mg, 31%) as an oil. Used without further characterization.

後処理

  1. temperatureto warm to room temperature
  2. extractionOrganics were extracted with 1:1 ether/hexanes (3×30 mL)
  3. washwashed with water (2×30 mL, brine (30 mL)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. washThe crude residue was subjected to chromatography on silica gel with gradient elution (5-20% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-c4f0385284df4279a0d4347739bb5c17
出典データセット
uspto-grants-2016_04
特許番号
US09315495B2

反応ノート

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