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Sulfuric Acid → HCID 22262058、化合物

HRID 406351
ノート
印刷プレビュー

反応式

HRID 406351 の反応式
Cl[CH2:2][C:3]([CH3:5])=[CH2:4].[CH:6]1[C:11]([OH:12])=[CH:10][CH:9]=[C:8]([CH3:13])[CH:7]=1.S(=O)(=O)(O)O.[OH-].[Na+]>COC(C)(C)C>[CH3:4][C:3]1([CH3:5])[C:10]2[CH:9]=[C:8]([CH3:13])[CH:7]=[CH:6][C:11]=2[O:12][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 1118Sulfuric AcidHCID 2879P-CresolHCID 112413-Chloro-2-methyl-1-propeneHCID 14798Sodium Hydroxide2 回

生成物 1

HCID 22262058HCID 22262058、化合物

試薬・触媒・溶媒 1

HCID 15413tert-Butyl methyl ether溶媒

実験手順

3-Chloro-2-methylpropene (9.7 mL) was added dropwise to a mixed solution of p-cresol (CAS #106-44-5, 10.8 g) and concentrated sulfuric acid (2.5 g), and the mixture was stirred at room temperature for one hour and 20 minutes. The reaction solution was ice-cooled and a 5 N sodium hydroxide aqueous solution (20 mL) was added, followed by stirring at 90° C. for 45 minutes. A 5 N sodium hydroxide aqueous solution (10 mL) was added to the reaction solution, and the mixture was stirred at 90° C. for two hours and 45 minutes. The reaction solution was left to cool to room temperature. tert-Butyl methyl ether was added to the reaction solution, and the organic layer was separated. The resulting organic layer was sequentially washed with water (three times) and brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (carrier: Merck silica gel 60 (230-400 mesh); elution solvent:heptane:ethyl acetate=1:0→49:1). The target fraction was concentrated and the resulting residue was purified again by silica gel column chromatography (carrier: Chromatorex™ NH; elution solvent: heptane). The target fraction was concentrated and the resulting residue was distilled under reduced pressure to obtain 1.87 g of the target compound (bp. 102° C./20 mmHg). The property values of the compound are as follows.

後処理

  1. temperaturecooled
  2. stirringby stirring at 90° C. for 45 minutes
  3. stirringthe mixture was stirred at 90° C. for two hours and 45 minutes
  4. waitThe reaction solution was left
  5. temperatureto cool to room temperature
  6. customthe organic layer was separated
  7. washThe resulting organic layer was sequentially washed with water (three times) and brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customThe resulting residue was purified by silica gel column chromatography (carrier: Merck silica gel 60 (230-400 mesh); elution solvent:heptane:ethyl acetate=1:0→49:1)
  11. concentrationThe target fraction was concentrated
  12. customthe resulting residue was purified again by silica gel column chromatography (carrier: Chromatorex™ NH; elution solvent: heptane)
  13. concentrationThe target fraction was concentrated
  14. distillationthe resulting residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-010e65e189344d8eb52fa8a59485c74c
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08754100B2

反応ノート

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