Diethyl Ether → 1,2,4-Benzenetriol

HRID 1902814

反応式

HRID 1902814 の反応式
C([O:4][C:5]1[CH:10]=[CH:9][C:8]([O:11]C(=O)C)=[CH:7][C:6]=1[O:15]C(=O)C)(=O)C.C(=O)([O-])[O-].[Na+].[Na+].C(OCC)C.S([O-])([O-])(=O)=O.[Na+].[Na+]>CO.S(=O)(=O)(O)O>[OH:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:6]=1[OH:15]

参加物

7

反応物 4

HCID 3283Diethyl EtherHCID 10340Sodium CarbonateHCID 24436Sodium SulfateHCID 691691,2,4-Triacetoxybenzene

生成物 1

HCID 107871,2,4-Benzenetriol

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 1118Sulfuric Acid溶媒

実験手順

Eighty grams of the crude 1,2,4-triacetoxybenzene were dissolved in 200 ml of methanol containing 6 g of concentrated sulfuric acid. The reaction mixture was boiled under reflux for one hour. Then the solution was cooled to room temperature and neutralized with an equivalent amount of fine powdered sodium carbonate. Thereafter 800 ml of ethylether was added whereupon sodium sulfate precipitated out, which was removed by filtration. Reaction by-products and contaminants being responsible for a dark red coloration may be removed employing solid silica gel. After evaporation of the supernatant under reduced pressure, a dark red oil is obtained which crystallized upon standing at 40° C. in the form of a slight reddish solid mass which is pure enough for the next step. This product is 1,2,4-trihydroxybenzene.

後処理

  1. temperatureunder reflux for one hour
  2. customprecipitated out
  3. customwhich was removed by filtration
  4. customReaction by-products and contaminants
  5. custommay be removed
  6. customAfter evaporation of the supernatant under reduced pressure
  7. customa dark red oil is obtained which
  8. customcrystallized
  9. customupon standing at 40° C. in the form of a slight reddish solid mass which

出典と根拠

ORDレコード
ord-694ef1eba17d4e9eb9c518b1ed3fdd7a
出典データセット
uspto-grants-1982_12
特許番号
US04366082

関連ノート

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