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Hydrazine hydrate (1:1) → 2-Methoxy-2-(naphthalen-2-yl)acetohydrazide

HRID 388253
ノート
印刷プレビュー

反応式

HRID 388253 の反応式
[CH3:1][O:2][CH:3]([C:8]1[CH:17]=[CH:16][C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=1)[C:4](OC)=[O:5].O.[NH2:19][NH2:20]>>[CH3:1][O:2][CH:3]([C:8]1[CH:17]=[CH:16][C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=1)[C:4]([NH:19][NH2:20])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 302866Methyl 2-methoxy-2-(naphthalen-2-yl)acetate

生成物 1

HCID 591858932-Methoxy-2-(naphthalen-2-yl)acetohydrazide収率 47%

実験手順

A stirred solution of methyl 2-methoxy-2-(naphthalen-2-yl)acetate (0.358 g, 1 eq) and hydrazine hydrate (4 mL) was heated to reflux for 1 hour. The reaction mixture was then cooled and the solvents removed under reduced pressure. The crude oil was diluted with EtOAc and washed with H2O and the organic phase dried over Na2SO4, filtered, and the solvents removed under reduced pressure to yield a yellow oil (0.17 g, 47%) that was used without further purification.

後処理

  1. temperatureto reflux for 1 hour
  2. temperatureThe reaction mixture was then cooled
  3. customthe solvents removed under reduced pressure
  4. additionThe crude oil was diluted with EtOAc
  5. washwashed with H2O
  6. dry with materialthe organic phase dried over Na2SO4
  7. filtrationfiltered
  8. customthe solvents removed under reduced pressure

出典と根拠

ORDレコード
ord-65ac9737f1d540dfbe5bac6e84ee52fe
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08377930B2

反応ノート

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