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Sulfuric Acid → 2-Phenoxyethyl 3-hydroxybenzoate

HRID 2220030
ノート
印刷プレビュー

反応式

HRID 2220030 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[O:11]([CH2:18][CH2:19]O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.S(=O)(=O)(O)O>>[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([O:7][CH2:19][CH2:18][O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:6]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 1118Sulfuric AcidHCID 74203-Hydroxybenzoic AcidHCID 31236Phenoxyethanol

生成物 1

HCID 135053562-Phenoxyethyl 3-hydroxybenzoate

反応条件

温度
95 °C

実験手順

Into a 250 mL round bottom flask equipped with magnetic stirrer and heating mantle was added 16.0 parts of 3-hydroxy benzoic acid, 100 parts of 2-phenoxyethanol and 0.5 parts of concentrated sulfuric acid. The reaction mixture was heated at 95° C. for 48 hours. The excess of 2-phenoxyethanol was evaporated under reduced pressure at 90° C. The solid material was dissolved in 250 mL of ethyl acetate. The organic layer was first washed with 200 mL of water, second with 250 mL of 5% solution of sodium bicarbonate in water and finally washed with 3×250 mL of water. The ethyl acetate layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. This material was purified by chromatography on silica gel using 20% ethyl acetate/hexane. The desired fractions were combined and solvent was evaporated to give an oily material which on treatment with hexane gave a solid, yield 5.1 parts. TLC on silica gel plate showed single spot. The structure of the product was confirmed on the basis of 1H NMR. The reaction proceeded as follows:

後処理

  1. customInto a 250 mL round bottom flask equipped with magnetic stirrer
  2. temperatureheating mantle
  3. customThe excess of 2-phenoxyethanol was evaporated under reduced pressure at 90° C
  4. dissolutionThe solid material was dissolved in 250 mL of ethyl acetate
  5. washThe organic layer was first washed with 200 mL of water, second with 250 mL of 5% solution of sodium bicarbonate in water
  6. washfinally washed with 3×250 mL of water
  7. dry with materialThe ethyl acetate layer was dried over anhydrous sodium sulfate
  8. customthe solvent was evaporated under reduced pressure
  9. customThis material was purified by chromatography on silica gel using 20% ethyl acetate/hexane
  10. customsolvent was evaporated
  11. customto give an oily material which on treatment with hexane
  12. customgave a solid
  13. customyield 5.1 parts

出典と根拠

ORDレコード
ord-e67268e14c5b41a2a072be29f9e5c28f
出典データセット
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07416898B2

反応ノート

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