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Methanol → Methyl (alphaR)-2-chloro-alpha-hydroxybenzeneacetate

HRID 1474568
ノート
印刷プレビュー

反応式

HRID 1474568 の反応式
[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C@@H:4]([OH:8])[C:5]([OH:7])=[O:6].P(=O)(Cl)(Cl)Cl.[CH3:18]O>>[Cl:1][C:2]1[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C@@H:4]([OH:8])[C:5]([O:7][CH3:18])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 24813Phosphorus oxychlorideHCID 2733641(-)-2-Chloromandelic acid

生成物 1

HCID 11790232Methyl (alphaR)-2-chloro-alpha-hydroxybenzeneacetate収率 95%

実験手順

15 g of (R)-2-chloromandelic acid was mixed with methanol (CH3OH, 150 ml) and phosphorus chloride oxide (POCl3, 0.76 ml) in a flask by stirring using a magnetic stirrer at the room temperature for 6 hours. When the reaction was completed, the obtained product was washed with an aqueous solution of sodium sulfite (Na2SO3) and ethylacetate (EA). Then, the organic layer was dehydrated with anhydrous magnesium sulfate (MgSO4), filtrated, and concented under reduced pressure. The concentrated residue was purified by a silica gel column chromatography to produce the title compound (15.64 g, yield 95%).

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  1. customat the room temperature
  2. customfor 6 hours
  3. washthe obtained product was washed with an aqueous solution of sodium sulfite (Na2SO3) and ethylacetate (EA)
  4. filtrationfiltrated
  5. customThe concentrated residue was purified by a silica gel column chromatography

出典と根拠

ORDレコード
ord-d6d2c917190442e683e90b3c2a10e3f9
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09018253B2

反応ノート

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