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Dimethyl Sulfoxide → 2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde

HRID 593434
ノート
印刷プレビュー

反応式

HRID 593434 の反応式
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH3:11][C:12]1([CH3:19])[O:16][CH:15]([CH2:17][OH:18])[CH2:14][O:13]1.O>C(Cl)Cl>[CH3:11][C:12]1([CH3:19])[O:16][CH:15]([CH:17]=[O:18])[CH2:14][O:13]1
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

6

反応物 4

HCID 679Dimethyl SulfoxideHCID 962WaterHCID 7528SolketalHCID 65578Oxalyl chloride

生成物 1

HCID 1107022,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒4 回

反応条件

温度
-60 °C

実験手順

A solution of anhydrous DMSO (3.41 mL, 48 mmol) in CH2Cl2 (5 mL) was added dropwise to a stirred solution of oxalyl chloride (1.92 mL, 22 mmol) in CH2Cl2 (50 mL) at −60° C. To this mixture was added a solution of (2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol (2.48 mL, 20 mmol) in CH2Cl2 (10 mL). The resulting mixture was stirred for 15 min at −60° C. TEA (13.9 mL, 100 mmol) was added dropwise. The reaction mixture was then warmed to room temperature. Water (50 mL) and CH2Cl2 (50 mL) were added. The organic layer was separated and washed with water (25 mL). The aqueous layer was extracted with CH2Cl2 (3×50 mL). The organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure to afford the crude 2,2-dimethyl-1,3-dioxolane-4-carbaldehyde that was used directly without further purification.

後処理

  1. temperatureThe reaction mixture was then warmed to room temperature
  2. customThe organic layer was separated
  3. washwashed with water (25 mL)
  4. extractionThe aqueous layer was extracted with CH2Cl2 (3×50 mL)
  5. dry with materialThe organic layers were dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-cb8ab75ac5b34eb38eb55a4c4112ef1c
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242964B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート