tert-Butanol → 4-tert-Butyl-3-chlorophenol

HRID 1165443

반응식

HRID 1165443 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.[CH3:9][C:10](O)([CH3:12])[CH3:11]>CCCCCC.P(=O)(O)(O)O>[Cl:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][C:7]=1[C:10]([CH3:12])([CH3:11])[CH3:9]

참가 물질

5

반응물 2

HCID 6386tert-ButanolHCID 79333-Chlorophenol

생성물 1

HCID 134994724-tert-Butyl-3-chlorophenol수율 0.6%

시약·촉매·용매 2

HCID 1004Phosphoric Acid용매HCID 8058Hexane용매2회

실험 절차

A mixture of 50 g (0.39 mol) of 3-chlorophenol in 250 ml of hexane and 125 ml of 85% phosphoric acid was heated to reflux. A solution of 43.2 g (0.584 mol) of 2-methyl-2-propanol in 25 ml of hexane was added over 1.5 hours. After addition, the reaction mixture was refluxed for 4 hours. The organic phase was separated and extracted four times with 30 ml of lN sodium hydroxide solution. The combined aqueous fractions were made acidic and extracted with methylene chloride. The organic phase was dried and evaporated at 90° C. (25 mm). The residue was crystallized from hexane. There was obtained 0.46 g (2.49 mmol, 0.6%) of 3-chloro-4-(1,1-dimethylethyl)phenol as a white solid after crystallization from hexane; mp 65°-67° C.

후처리

  1. temperaturewas heated to reflux
  2. additionAfter addition
  3. temperaturethe reaction mixture was refluxed for 4 hours
  4. customThe organic phase was separated
  5. extractionextracted four times with 30 ml of lN sodium hydroxide solution
  6. extractionextracted with methylene chloride
  7. customThe organic phase was dried
  8. customevaporated at 90° C. (25 mm)
  9. customThe residue was crystallized from hexane

출처 및 근거

ORD 기록
ord-807a84e578c14241bdcb3dfe71f4655f
출처 데이터셋
uspto-grants-1990_03
특허 번호
US04910202

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