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Hydrogen Peroxide → (1S)-1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carboxamide

HRID 2056723
ノート
印刷プレビュー

反応式

HRID 2056723 の反応式
[OH:1][CH2:2][CH2:3][C@H:4]1[C:9]2[CH:10]=[CH:11][C:12]([C:14]#[N:15])=[CH:13][C:8]=2[CH2:7][CH2:6][O:5]1.C(=O)([O-])[O-:17].[K+].[K+].OO.C(OCC)(=O)C>CO.CS(C)=O.O>[OH:1][CH2:2][CH2:3][C@H:4]1[C:9]2[CH:10]=[CH:11][C:12]([C:14]([NH2:15])=[O:17])=[CH:13][C:8]=2[CH2:7][CH2:6][O:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 784Hydrogen PeroxideHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 69306499(1S)-1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carbonitrile

生成物 1

HCID 69308374(1S)-1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carboxamide

試薬・触媒・溶媒 3

HCID 679
Dimethyl Sulfoxide
溶媒
HCID 887Methanol溶媒
HCID 962Water溶媒

実験手順

To a solution of crude (1S)-1-(2-hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carbonitrile (178 g, 0.88 mol) in methanol (460 mL) and DMSO (125 mL) was added potassium carbonate (13 g, 94 mmol). 35% hydrogen peroxide (102 mL) was then added dropwise while maintaining the temperature of the mixture below 50° C. The reaction mixture was then allowed to stir for 1 h at ambient temperature. Analysis of an aliquot by silica TLC (ethyl acetate) indicated that the reaction was complete. Water (130 mL) was added and methanol removed in vacuo. Water (800 mL) and 1N HCl (100 mL) were added and the mixture allowed to stir overnight. The solid was filtered, washed with water, and dried. Recrystallization from methyl(i-butyl)ketone gave the title compound.

後処理

  1. temperaturewhile maintaining the temperature of the mixture below 50° C
  2. custommethanol removed in vacuo
  3. additionWater (800 mL) and 1N HCl (100 mL) were added
  4. stirringto stir overnight
  5. filtrationThe solid was filtered
  6. washwashed with water
  7. customdried
  8. customRecrystallization from methyl(i-butyl)ketone

出典と根拠

ORDレコード
ord-3a6f00b36b2c48459a05aa89c3c2a8e1
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07335660B2

反応ノート

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