Hydrochloric Acid → 5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedimethanol

HRID 1732077

反応式

HRID 1732077 の反応式
[OH-:1].[Na+].[C:3]([C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1)([CH3:6])([CH3:5])[CH3:4].[C:14]1([OH:20])C=CC=CC=1.[CH2:21]=O.Cl>O.C(Cl)(Cl)Cl>[C:3]([C:7]1[CH:8]=[C:9]([CH2:21][OH:1])[C:10]([OH:13])=[C:11]([CH2:14][OH:20])[CH:12]=1)([CH3:6])([CH3:4])[CH3:5]

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 712FormaldehydeHCID 996PhenolHCID 73934-tert-ButylphenolHCID 14798Sodium Hydroxide

生成物 1

HCID 1509815-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedimethanol

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6212Chloroform溶媒

実験手順

50 g sodium hydroxide were dissolved in approximately 1.2 liters of water, and 150 g of 4-tert-butylphenol were added to this solution. The mixture was stirred and gently heated until the phenol dissolved. The solution was then cooled to ambient temperature. Aqueous formaldehyde (175 ml, 37 percent) was added, and the solution was stirred for four to six days at ambient temperature. Concentrated hydrochloric acid (110 ml) was added, upon which a two-phase system formed. A yellow, oily organic phase was isolated and washed with three 500 ml portions of water. Chloroform (700 ml) and 500 ml of water were added to this organic oil and the mixture was stirred. The organic phase was isolated and dried over 100 g of anhydrous magnesium sulphate. Evaporation and cooling of the chloroform solution yielded a mixture of white crystals and oil. The addition of 50-100 ml of chloroform and filtration yielded a white crystalline product, 4-tert-butyl-2,6-di(hydroxymethyl) phenol.

後処理

  1. dissolutiondissolved
  2. stirringthe solution was stirred for four to six days at ambient temperature
  3. customformed
  4. customA yellow, oily organic phase was isolated
  5. washwashed with three 500 ml portions of water
  6. additionChloroform (700 ml) and 500 ml of water were added to this organic oil
  7. stirringthe mixture was stirred
  8. customThe organic phase was isolated
  9. dry with materialdried over 100 g of anhydrous magnesium sulphate
  10. customEvaporation
  11. temperaturecooling of the chloroform solution
  12. customyielded
  13. additiona mixture of white crystals and oil

出典と根拠

ORDレコード
ord-6003f13efc7a400eb13e84725c93c994
出典データセット
uspto-grants-1986_11
特許番号
US04625002

関連ノート

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