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Triethylamine → Methyl 8-{[(5-bromo-2-methylphenyl)acetyl]amino}-1,4-dioxaspiro[4.5]decane-8-carboxylate

HRID 922128
ノート
印刷プレビュー

反応式

HRID 922128 の反応式
[NH2:1][C:2]1([C:12]([O:14][CH3:15])=[O:13])[CH2:11][CH2:10][C:5]2([O:9][CH2:8][CH2:7][O:6]2)[CH2:4][CH2:3]1.C(N(CC)CC)C.[Br:23][C:24]1[CH:25]=[CH:26][C:27]([CH3:34])=[C:28]([CH2:30][C:31](Cl)=[O:32])[CH:29]=1>ClCCl>[Br:23][C:24]1[CH:25]=[CH:26][C:27]([CH3:34])=[C:28]([CH2:30][C:31]([NH:1][C:2]2([C:12]([O:14][CH3:15])=[O:13])[CH2:3][CH2:4][C:5]3([O:9][CH2:8][CH2:7][O:6]3)[CH2:10][CH2:11]2)=[O:32])[CH:29]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 12182743Methyl 8-amino-1,4-dioxaspiro[4.5]decane-8-carboxylateHCID 51063875(5-Bromo-2-methylphenyl)acetyl chloride

生成物 1

HCID 67375909Methyl 8-{[(5-bromo-2-methylphenyl)acetyl]amino}-1,4-dioxaspiro[4.5]decane-8-carboxylate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒3 回

実験手順

At room temperature, 5.47 g (25.41 mmol) of methyl 8-amino-1,4-dioxaspiro[4.5]decane-8-carboxylate [T. Satoh et al., Tetrahedron 63 (2007), 4806-4813], 3.86 g (38.12 mmol) of triethylamine and 155 mg (1.27 mmol) of N,N-dimethylaminopyridine were dissolved in 45 ml of dichloromethane. A solution of 6.29 g (25.41 mmol) of (5-bromo-2-methylphenyl)acetyl chloride (Example 3A) in 45 ml of dichloromethane was then added dropwise to the mixture. The resulting reaction mixture was stirred at room temperature overnight. For work-up, the mixture was diluted with dichloromethane and the organic phase was washed with aqueous saturated sodium bicarbonate solution. After drying over sodium sulphate, the mixture was concentrated by evaporation and the residue was purified by chromatography on silica gel (mobile phase: hexane/ethyl acetate gradient/1% triethylamine) Evaporation and drying gave 3.64 g (34% of theory) of the title compound which was used without further characterization in the next step.

後処理

  1. customThe resulting reaction mixture
  2. washthe organic phase was washed with aqueous saturated sodium bicarbonate solution
  3. dry with materialAfter drying over sodium sulphate
  4. concentrationthe mixture was concentrated by evaporation
  5. customthe residue was purified by chromatography on silica gel (mobile phase: hexane/ethyl acetate gradient/1% triethylamine) Evaporation
  6. customdrying

出典と根拠

ORDレコード
ord-9fea5488ddf540c19d5aef1337df0d66
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09278925B2

反応ノート

読み込み中…

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