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Hydrochloric Acid → 4-Formyl-2-pentyl-benzoic acid methyl ester

HRID 2261805
ノート
印刷プレビュー

反応式

HRID 2261805 の反応式
[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]2OCC=C[O:11]2)=[CH:6][C:5]=1[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20].Cl>C1COCC1>[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[O:11])=[CH:6][C:5]=1[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]
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 2

HCID 313Hydrochloric AcidHCID 675283664-[1,3]Dioxin-2-yl-2-pentyl-benzoic acid methyl ester

生成物 1

HCID 574433334-Formyl-2-pentyl-benzoic acid methyl ester収率 98%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 4-[1,3]Dioxin-2-yl-2-pentyl-benzoic acid methyl ester (360 mg, 1.3 mmol) in THF (5.0 mL) is added concentrated HCl (0.55 mL, 6.5 mmol). The reaction is stirred for 2.0 h. The reaction mixture is partitioned between EtOAc (20 mL) and water (20 mL). The organic phase is washed with brine (20 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to a residue. The residue is purified by flash chromatography to afford the title compound as syrup (236 mg, 98%). LC-ES/MS m/e 235.3 (M+1).

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 reaction mixture is partitioned between EtOAc (20 mL) and water (20 mL)
  2. washThe organic phase is washed with brine (20 mL)
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure to a residue
  6. customThe residue is purified by flash chromatography

出典と根拠

ORDレコード
ord-b6cc4ca4ce1f4a4592f6788590ebba7c
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07846960B2

反応ノート

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