Water → (1-Benzylcyclohex-2-en-1-yl)acetic acid

HRID 901825ノート

反応式

HRID 901825 の反応式
[O-]Cl=O.[Na+].[OH2:5].[CH2:6]([C:13]1([CH2:19][CH:20]=[O:21])[CH2:18][CH2:17][CH2:16][CH:15]=[CH:14]1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>CS(C)=O.CCOCC>[CH2:6]([C:13]1([CH2:19][C:20]([OH:5])=[O:21])[CH2:18][CH2:17][CH2:16][CH:15]=[CH:14]1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

参加物

6

反応物 3

HCID 962WaterHCID 22243087(1-Benzylcyclohex-2-en-1-yl)acetaldehydeHCID 23668197Sodium Chlorite

生成物 1

HCID 22243083(1-Benzylcyclohex-2-en-1-yl)acetic acid

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒2 回HCID 3283Diethyl Ether溶媒

反応条件

温度
0 °C

実験手順

To a mixture of NaH2PO4 (55.3 g), NaClO2 (36.3 g), DMSO (200 mL) and water (375 mL) was added a solution of 3-benzyl-3-formylmethylcyclohexene (57 g) in DMSO (150 mL) during a 3 hour period. After addition, the mixture was stirred overnight and diluted with ether (200 mL). This was extracted with saturated NaHCO3 (3×100 mL). The combined aqueous layer was cooled to 0° C. and acidified to PH=1 with conc. HCl. This was extracted with CH2Cl2 (3×300 mL). The combined organic layer was dried (Na2SO4) and the solvent was removed in vacuo. The residue was purified by column chromatography on silica gel to give the title compound as thick oil (50 g). MS (MH+=231).

後処理

  1. additionAfter addition
  2. extractionThis was extracted with saturated NaHCO3 (3×100 mL)
  3. extractionThis was extracted with CH2Cl2 (3×300 mL)
  4. dry with materialThe combined organic layer was dried (Na2SO4)
  5. customthe solvent was removed in vacuo
  6. customThe residue was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-77aebeed3e144ef19963ab7ffe38b146
出典データセット
uspto-grants-2008_04
特許番号
US07365062B2

反応ノート

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