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Iodine → 2-Propyl-3-t-butyl-4-hydroxy-5-isopropylphenol

HRID 327324
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반응식

HRID 327324 반응식
[CH2:1]([C:4]1[C:5](=[O:18])[CH:6]=[C:7]([CH:15]([CH3:17])[CH3:16])[C:8](=[O:14])[C:9]=1[C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:2][CH3:3].C[SiH](C)O[SiH](C)C.II>C(Cl)Cl>[CH2:1]([C:4]1[C:9]([C:10]([CH3:12])([CH3:11])[CH3:13])=[C:8]([OH:14])[C:7]([CH:15]([CH3:17])[CH3:16])=[CH:6][C:5]=1[OH:18])[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 807IodineHCID 186591,1,3,3-Tetramethyl-disiloxaneHCID 570664232-Propyl-3-t-butyl-5-isopropylbenzoquinone

생성물 1

HCID 540178862-Propyl-3-t-butyl-4-hydroxy-5-isopropylphenol

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Dissolve 2-propyl-3-t-butyl-5-isopropylbenzoquinone (10mmol), 1,1,3,3-tetramethyldisiloxane (1.79mL, 10mmol) and iodine (0.05g) in methylene chloride (30mL). Stir at reflux for 30 minutes and extract with 1N sodium hydroxide (30mL). Acidify the aqueous phase with concentrated hydrochloric acid and extract into ethyl acetate (4×10mL), dry (NazSO4) and evaporate the solvent in vacuo to give 2-propyl-3-t-butyl-4-hydroxy-5-isopropylphenol.

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후처리

  1. temperatureat reflux for 30 minutes
  2. extractionextract with 1N sodium hydroxide (30mL)
  3. extractionextract into ethyl acetate (4×10mL)
  4. customdry (NazSO4)
  5. customevaporate the solvent in vacuo

출처 및 근거

ORD 기록
ord-b46a9b0399e14315810fcbac9dd0be5b
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05272252

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