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Sodium Hydroxide → HCID 69311668、化合物

HRID 33223
ノート
印刷プレビュー

反応式

HRID 33223 の反応式
C[O:2][C:3](=[O:13])[CH2:4][CH2:5][CH2:6][CH:7]1[O:12][CH2:11][CH2:10][CH2:9][O:8]1.[OH-].[Na+]>O.CO>[O:8]1[CH2:9][CH2:10][CH2:11][O:12][CH:7]1[CH2:6][CH2:5][CH2:4][C:3]([OH:13])=[O:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14798Sodium HydroxideHCID 693128054-[1,3]Dioxan-2-yl-butyric acid methyl ester

生成物 1

HCID 69311668HCID 69311668、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

4-[1,3]Dioxan-2-yl-butyric acid methyl ester (6.8 g, 0.036 mol) was added to a stirred solution of sodium hydroxide (1.87 g, 0.047 mol) in water (30 ml) and methanol (30 ml). The mixture was stirred for 18 h at room temperature and then the solvent evaporated. The residue was partitioned between ethyl acetate (100 ml) and water (100 ml) and cooled to 0° C. The mixture was acidified with hydrochloric acid (1M) to pH 2 and the layers separated. The aqueous layer was further extracted with cold ethyl acetate (100 ml) and the combined organic layers washed with brine (100 ml) and then dried (Na2SO4). The solvents were evaporated and the crude solid (5.56 g) was used in the next step.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customthe solvent evaporated
  2. customThe residue was partitioned between ethyl acetate (100 ml) and water (100 ml)
  3. temperaturecooled to 0° C
  4. customthe layers separated
  5. extractionThe aqueous layer was further extracted with cold ethyl acetate (100 ml)
  6. washthe combined organic layers washed with brine (100 ml)
  7. dry with materialdried (Na2SO4)
  8. customThe solvents were evaporated

出典と根拠

ORDレコード
ord-c63079a6f7f1435894ec7d9308a93c8f
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07429579B2

反応ノート

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