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Acetic Acid → 4-(2-Methylpropyl)-1,2-benzenediol

HRID 704005
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HRID 704005 반응식
[CH2:1]([C:5]1[CH:6]=[C:7]([O:13]C)[C:8]([O:11]C)=[CH:9][CH:10]=1)[CH:2]([CH3:4])[CH3:3].C(O)(=O)C.Br>O>[CH2:1]([C:5]1[CH:6]=[C:7]([OH:13])[C:8](=[CH:9][CH:10]=1)[OH:11])[CH:2]([CH3:4])[CH3:3]
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참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 260Hydrogen BromideHCID 14372664HCID 14372664, 화합물

생성물 1

HCID 143726654-(2-Methylpropyl)-1,2-benzenediol수율 82%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 50.83 g (262 mM) of 4-iso-butylveratrole, 167.82 g (2.795 mM) of acetic acid and 502.18 g (2.917 mM) of 47% hydrobromic acid was heated under reflux for 19 hours with stirring. The reaction mixture was cooled to the room temperature added with 400 ml of water. The separated oil was extracted with ether. The ether solution was successively washed with 400 ml of water, 660 g of 5% aqueous sodium thiosulfate solution, and further twice with each 400 ml of water. The resulting solution was dried with anhydrous sodium sulfate, distilled off ether, and vacuum distilled to obtain 35.68 g (215 mM) of 4-iso-butylcatechol as yellow viscous liquid having a boiling point of 117°-120° C./ 2 mmHg.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 19 hours
  3. extractionThe separated oil was extracted with ether
  4. washThe ether solution was successively washed with 400 ml of water, 660 g of 5% aqueous sodium thiosulfate solution
  5. dry with materialThe resulting solution was dried with anhydrous sodium sulfate
  6. distillationdistilled off ether, and vacuum
  7. distillationdistilled

출처 및 근거

ORD 기록
ord-3c10f14ad2c047f385ad774ea06a8220
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04985458

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