Ammonia → (3-((Tert-butyldimethylsilyloxy)methyl)phenyl)methanol

HRID 505677

反応式

HRID 505677 の反応式
[C:1]1([CH2:9][OH:10])[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][OH:8])[CH:2]=1.C(N(CC)CC)C.[C:18]([Si:22]([CH3:25])([CH3:24])Cl)([CH3:21])([CH3:20])[CH3:19].N>ClCCl>[Si:22]([O:8][CH2:7][C:3]1[CH:2]=[C:1]([CH2:9][OH:10])[CH:6]=[CH:5][CH:4]=1)([C:18]([CH3:21])([CH3:20])[CH3:19])([CH3:25])[CH3:24]

参加物

6

反応物 4

HCID 222AmmoniaHCID 8471TriethylamineHCID 28928tert-Butyldimethylsilyl chlorideHCID 693741,3-Benzenedimethanol

生成物 1

HCID 10658493(3-((Tert-butyldimethylsilyloxy)methyl)phenyl)methanol収率 45.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To 1,3-benzenedimethanol (5.10 g, 36.91 mmol) in dichloromethane (70 ml) was added at 0° C. triethylamine (7.47 g, 73.82 mmol), 4-dimethyl-aminopyridine (451 mg, 3.61 mmol) and t-butyldimethylchlorosilane (5.56 g, 36.91 mmol) successively, and the mixture was stirred for 20 hours at room temperature. Thereto was added a saturated ammonia solution and the mixture was extracted with ethyl acetate and separated by a separating funnel. The organic layer was washed with water and saturated brine, dried over magnesium sulfate and filtered. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give the subject compound (4.23 g, 45%).

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. customseparated by a separating funnel
  3. washThe organic layer was washed with water and saturated brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customThe solvent was removed in vacuo
  7. customthe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-50fc8bbb3b3b47048f33b51ad57a2c25
出典データセット
uspto-grants-2010_08
特許番号
US07781479B2

関連ノート

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