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Hydrogen Peroxide → 5-fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrile

HRID 2173247
ノート
印刷プレビュー

反応式

HRID 2173247 の反応式
[F:1][C:2]1[CH:10]=[CH:9][C:8]2[C:7](=[CH2:11])[CH2:6][CH2:5][C:4]=2[C:3]=1[C:12]#[N:13].B.C1C[O:18]CC1.[OH-].[Na+].OO>C1COCC1.O>[F:1][C:2]1[CH:10]=[CH:9][C:8]2[CH:7]([CH2:11][OH:18])[CH2:6][CH2:5][C:4]=2[C:3]=1[C:12]#[N:13]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 2723981Borane;tetrahydrofuranHCID 684320125-fluoro-1-methylidene-2,3-dihydro-1H-indene-4-carbonitrile

生成物 1

HCID 666463905-fluoro-1-(hydroxymethyl)-2,3-dihydro-1H-indene-4-carbonitrile

試薬・触媒・溶媒 2

HCID 962Water
溶媒
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

To a solution of 5-Fluoro-1-methylidene-2,3-dihydro-1H-indene-4-carbonitrile (30 mg, 0.173 mmol) in THF was added BH3.THF (0.173 ml, 0.173 mmol) at 0° C. The mixture was allowed to stir at 0° C. for 15 minutes, and then warm up to RT for 30 minutes. TLC showed little SM left at that point. To this reaction was then added Sodium Hydroxide (2M, 0.173 ml, 0.346 mmol) and Hydrogen peroxide (39.3 mg, 0.346 mmol). The mixture was stirred for another hour at RT. TLC and LC showed good reaction. The reaction was diluted with water, extracted with EtOAc, washed with water and brine, dried over Na2SO4, and concentrated. The resulting oil was used directly in the next step. LC-MS (IE, m/z): 192 [M+1]+.

後処理

  1. temperaturewarm up to RT for 30 minutes
  2. waitleft at that point
  3. stirringThe mixture was stirred for another hour at RT
  4. customreaction
  5. extractionextracted with EtOAc
  6. washwashed with water and brine
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-40d01cc91c254946ac1c82ad3e39822c
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09056859B2

反応ノート

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