Dimethyl Sulfoxide → 2-benzyloxy-3-methylbenzaldehyde

HRID 717385ノート

反応式

HRID 717385 の反応式
[CH2:1]([O:8][C:9]1[C:14]([CH3:15])=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:16][OH:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CS(C)=O.I(C1C=CC=CC=1C(O)=O)(=O)=O>C(OCC)(=O)C>[CH2:1]([O:8][C:9]1[C:14]([CH3:15])=[CH:13][CH:12]=[CH:11][C:10]=1[CH:16]=[O:17])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

5

反応物 3

HCID 679Dimethyl SulfoxideHCID 1087942-Iodoxybenzoic acidHCID 14265632HCID 14265632、化合物

生成物 1

HCID 110641372-benzyloxy-3-methylbenzaldehyde

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

Into a 500-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed [2-(benzyloxy)-3-methylphenyl]methanol (30 g, 131.41 mmol, 1.00 equiv) and DMSO (300 mL). This was followed by the addition of 2-iodoxybenzoic acid (41 g, 146.42 mmol, 1.10 equiv) in several batches. The resulting solution was stirred for 2 h at room temperature. The resulting solution was diluted with 1.5 L of ethyl acetate. The resulting mixture was washed with 3×800 mL of brine. The mixture was dried over anhydrous sodium sulfate. This resulted in 30 g (crude) of 2-(benzyloxy)-3-methylbenzaldehyde as orange oil. MS (ESI) m/z 227 ([M+H]).

後処理

  1. customInto a 500-mL 3-necked round-bottom flask purged
  2. temperaturemaintained with an inert atmosphere of nitrogen
  3. washThe resulting mixture was washed with 3×800 mL of brine
  4. dry with materialThe mixture was dried over anhydrous sodium sulfate
  5. customThis resulted in 30 g (crude) of 2-(benzyloxy)-3-methylbenzaldehyde as orange oil

出典と根拠

ORDレコード
ord-5b07973a52e64e77aea9ebe346d46f76
出典データセット
uspto-grants-2015_11
特許番号
US09193707B2

反応ノート

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