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Sodium Hydroxide → 862501-94-8

HRID 555677
ノート
印刷プレビュー

反応式

HRID 555677 の反応式
[C:1]12([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:8][CH2:7][C:4]([C:9]([O:11]C)=[O:10])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2.[OH-].[Na+]>CO>[C:1]12([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:2][CH2:3][C:4]([C:9]([OH:11])=[O:10])([CH2:5][CH2:6]1)[CH2:7][CH2:8]2
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 2

HCID 14798Sodium HydroxideHCID 23149682HCID 23149682、化合物

生成物 1

HCID 23149699862501-94-8収率 73.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

1,1-Dimethylethyl methyl bicyclo[2.2.2]octane-1,4-dicarboxylate (495 mg) was dissolved in methanol (5 mL). To this solution, a 2 mol/L aqueous sodium hydroxide solution (0.92 mL) was added and the mixture was stirred at room temperature for 8 hours and then at 50° C. for 2 hours. Methanol in the mixture was evaporated under reduced pressure. Water was added to the resulting residue and the mixture was washed with diethyl ether and was neutralized with 3 mol/L hydrochloric acid. The resulting crystals were filtered, washed with water, and dried under reduced pressure to give 1,1-dimethylethyl hydrogen bicyclo[2.2.2]octane-1,4-dicarboxylate (344 mg).

後処理

  1. waitat 50° C. for 2 hours
  2. customMethanol in the mixture was evaporated under reduced pressure
  3. additionWater was added to the resulting residue
  4. washthe mixture was washed with diethyl ether
  5. filtrationThe resulting crystals were filtered
  6. washwashed with water
  7. customdried under reduced pressure

出典と根拠

ORDレコード
ord-4f4ac773b7d6430ab5c48f6e88e3463a
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08053465B2

反応ノート

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