Dimethyl Sulfoxide → Phenoxyacetaldehyde

HRID 397822

反応式

HRID 397822 の反応式
CS(C)=O.C(Cl)(=O)C(Cl)=O.[O:11]([CH2:18][CH2:19][OH:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C>C(Cl)Cl>[O:11]([CH2:18][CH:19]=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

参加物

6

反応条件

温度
-78 °C

実験手順

At −78° C., a solution of dimethylsulphoxide (5.11 ml, 72 mmol) in DCM (50 ml) was added dropwise to a solution of oxalyl chloride (6.12 ml, 72 mmol) in DCM (150 ml). The reaction mixture was stirred for 10 min at −78° C. A solution of 2-phenoxyethanol (10.0 g, 72 mmol) in DCM (70 ml) was added dropwise. The reaction mixture was stirred at −78° C. for 10 min. A solution of triethylamine (50 ml, 360 mmol) in DCM (50 ml) was added dropwise. The reaction mixture was stirred for 10 min at −78° C. It was warmed to room temperature. The reaction mixture was washed with a 10% aqueous solution of sodium hydrogensulphate (2×200 ml) and subsequently with brine (2×200 ml). It was dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (100 g), using ethyl acetate/heptane (1:3) as eluent, to give 2.73 g of phenoxyacetaldehyde.

後処理

  1. stirringThe reaction mixture was stirred at −78° C. for 10 min
  2. stirringThe reaction mixture was stirred for 10 min at −78° C
  3. temperatureIt was warmed to room temperature
  4. washThe reaction mixture was washed with a 10% aqueous solution of sodium hydrogensulphate (2×200 ml) and subsequently with brine (2×200 ml)
  5. dry with materialIt was dried over magnesium sulphate
  6. customThe solvent was removed in vacuo
  7. customThe crude product was purified by flash chromatography on silica (100 g)

出典と根拠

ORDレコード
ord-d6d469175cb644ea9ab1c070e103756f
出典データセット
uspto-grants-2003_08
特許番号
US06610721B2

関連ノート

読み込み中…