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5,7-dimethyl-8-methoxy-9-(2,2-diethoxyethyl)-1,2,3,4-tetrahydro-9H-fluorene → 5,7-dimethyl-8-methoxy-9-formylmethyl-1,2,3,4-tetrahydro-9H-fluorene

HRID 2051420
ノート
印刷プレビュー

反応式

HRID 2051420 の反応式
[CH3:1][C:2]1[CH:14]=[C:13]([CH3:15])[C:12]([O:16][CH3:17])=[C:11]2[C:3]=1[C:4]1[CH2:5][CH2:6][CH2:7][CH2:8][C:9]=1[CH:10]2[CH2:18][CH:19](OCC)[O:20]CC>O1CCCC1.Cl>[CH3:1][C:2]1[CH:14]=[C:13]([CH3:15])[C:12]([O:16][CH3:17])=[C:11]2[C:3]=1[C:4]1[CH2:5][CH2:6][CH2:7][CH2:8][C:9]=1[CH:10]2[CH2:18][CH:19]=[O:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 151572005,7-dimethyl-8-methoxy-9-(2,2-diethoxyethyl)-1,2,3,4-tetrahydro-9H-fluorene

生成物 1

HCID 151572015,7-dimethyl-8-methoxy-9-formylmethyl-1,2,3,4-tetrahydro-9H-fluorene収率 105.4%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A tetrahydrofuran solution containing 1.45 g of 5,7-dimethyl-8-methoxy-9-(2,2-diethoxyethyl)-1,2,3,4-tetrahydro-9H-fluorene in 10 ml of tetrahydrofuran and 10 ml of 15% hydrochloric acid were stirred at room temperature for 3 hours. The reaction mixture was extracted with dichloromethane and the extract was washed with saturated aqueous sodium chloride solution and saturated sodium bicarbonate solution and then dried with magnesium sulfate. The solvent was distilled off to obtain 1.20 g of 5,7-dimethyl-8-methoxy-9-formylmethyl-1,2,3,4-tetrahydro-9H-fluorene.

後処理

  1. extractionThe reaction mixture was extracted with dichloromethane
  2. washthe extract was washed with saturated aqueous sodium chloride solution and saturated sodium bicarbonate solution
  3. dry with materialdried with magnesium sulfate
  4. distillationThe solvent was distilled off

出典と根拠

ORDレコード
ord-640fd08a464d4fdab2c0473be67990b7
出典データセット
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05017724

反応ノート

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