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Hydrochloric Acid → Benzenepropanoic acid, 3-(1,1-dimethylethyl)-4-hydroxy-, methyl ester

HRID 1461890
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HRID 1461890 반응식
[C:1]([C:5]1[CH:6]=[C:7]([CH2:16][CH2:17][C:18]([O:20][CH3:21])=[O:19])[CH:8]=[C:9](C(C)(C)C)[C:10]=1[OH:11])([CH3:4])([CH3:3])[CH3:2].Cl>C1(C)C=CC=CC=1>[C:1]([C:5]1[CH:6]=[C:7]([CH2:16][CH2:17][C:18]([O:20][CH3:21])=[O:19])[CH:8]=[CH:9][C:10]=1[OH:11])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 62603Methyl di-t-butyl hydroxyhydrocinnamate

생성물 1

HCID 3084638Benzenepropanoic acid, 3-(1,1-dimethylethyl)-4-hydroxy-, methyl ester수율 71.8%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 50 g of methyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, 2.5 g of conc. hydrochloric acid and 30 ml of toluene was refluxed for 2 hours while stirring. After the completion of the reaction, the reaction mixture was washed with water and the solvent wa distilled off. Hexane was added to the residue and the mixture was icecooled. The resulting crystals were collected by filtration and recrystallized from hexane to give 29 g of methyl 3-(3-tert-butyl-4-hydroxyphenyl)propionate as white crystals, m.p. 59°-61° C.

후처리

  1. temperaturewas refluxed for 2 hours
  2. customAfter the completion of the reaction
  3. washthe reaction mixture was washed with water
  4. distillationthe solvent wa distilled off
  5. additionHexane was added to the residue
  6. filtrationThe resulting crystals were collected by filtration
  7. customrecrystallized from hexane

출처 및 근거

ORD 기록
ord-f941720abb724c46ac78a04023a1f2e3
출처 데이터셋
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05077424

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