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tert-Butanol → 1,1-Dimethylethyl 5-hexynoate

HRID 1482245
ノート
印刷プレビュー

反応式

HRID 1482245 の反応式
[C:1]([OH:8])(=[O:7])[CH2:2][CH2:3][CH2:4][C:5]#[CH:6].[CH3:9][C:10](O)([CH3:12])[CH3:11].C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C1C=CN=CC=1.C(Cl)Cl>[C:1]([O:8][C:10]([CH3:12])([CH3:11])[CH3:9])(=[O:7])[CH2:2][CH2:3][CH2:4][C:5]#[CH:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6386tert-ButanolHCID 10868DicyclohexylcarbodiimideHCID 1430365-Hexynoic acid

生成物 1

HCID 109649121,1-Dimethylethyl 5-hexynoate

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane溶媒2 回

実験手順

Hex-5-ynoic acid (Compound SP424) (8.0 g, 71.3 mmol), 2-methylpropan-2-ol (10.6 g, 143.0 mmol) and 4-(dimethylamino)pyridine (0.44 g, 3.60 mmol) were dissolved in DCM (17.5 ml), a solution of dicyclohexylcarbodiimide (16.2 g, 78.5 mmol) in DCM (17.5 ml) was added, and the mixture was stirred at room temperature overnight. The white solid in the reaction solution was removed by filtration, after which the filtrate was washed with a 0.5 M aqueous hydrochloric acid solution and a saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate. The residue obtained by filtration and concentration under reduced pressure was purified by column chromatography (hexane:ethyl acetate=100:0-90:10) to afford the title compound SP423 (6.73 g, 56.1%).

後処理

  1. customThe white solid in the reaction solution was removed by filtration
  2. washafter which the filtrate was washed with a 0.5 M aqueous hydrochloric acid solution
  3. dry with materiala saturated aqueous sodium bicarbonate solution and dried over anhydrous magnesium sulfate
  4. customThe residue obtained by filtration and concentration under reduced pressure
  5. customwas purified by column chromatography (hexane:ethyl acetate=100:0-90:10)

出典と根拠

ORDレコード
ord-09e679b9a2f641d6ab10361c5883f851
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409952B2

反応ノート

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