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Hydrochloric Acid → Acetaldehyde, 2-(4-bromo-2-methylphenoxy)-

HRID 2219229
ノート
印刷プレビュー

反応式

HRID 2219229 の反応式
Cl.[Br:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][CH:11](OC)[O:12]C)=[C:5]([CH3:16])[CH:4]=1.[Na+].[Cl-]>CCOCC>[Br:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][CH:11]=[O:12])=[C:5]([CH3:16])[CH:4]=1
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 3

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 196085464-Bromo-1-[(2,2-dimethoxyethyl)oxy]-2-methylbenzene

生成物 1

HCID 14816015Acetaldehyde, 2-(4-bromo-2-methylphenoxy)-収率 116.6%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

A 5N HCl (15 mL) solution is added to a stirred solution of 4-bromo-1-(2,2-dimethoxy-ethoxy)-2-methyl-benzene (1.40 g, 5.09 mmol) in Et2O (25 mL). The two-layered solution is stirred vigorously at ambient temperature under nitrogen for 2 days. Et2O (50 mL) and saturated aqueous NaCl solution (25 mL) are added to the mixture. The organic layer is separated, washed with a half-saturated aqueous NaCl solution (30 mL) containing saturated NaHCO3 (0.5 mL), dried over MgSO4, filtered and concentrated at ambient temperature to give 1.36 g of the crude (4-bromo-2-methyl-phenoxy)acetaldehyde as oil. The oil is diluted in Et2O to form a stock solution (67 mg/mL), which is used for the subsequent reaction.

後処理

  1. customThe organic layer is separated
  2. washwashed with a half-saturated aqueous NaCl solution (30 mL)
  3. additioncontaining saturated NaHCO3 (0.5 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated at ambient temperature

出典と根拠

ORDレコード
ord-36d53961a31b4a5580efbc5935d2a03d
出典データセット
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07414063B2

反応ノート

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