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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 2-(2-Bromo-3-methylphenyl)acetic acid

HRID 1006698
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HRID 1006698 반응식
[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[CH2:4][C:5]#N.S(=O)(=O)(O)[OH:13].[OH2:17]>C(OCC)C>[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[CH2:4][C:5]([OH:13])=[O:17]
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참가 물질

5

반응물 3

HCID 962Water2회HCID 1118Sulfuric AcidHCID 226726132-(2-Bromo-3-methylphenyl)acetonitrile

생성물 1

HCID 183574462-(2-Bromo-3-methylphenyl)acetic acid

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

2-bromo-3-methylbenzylcyanid (8.8 g, 42 mmol) was added to a mixture of conc sulfuric acid (50 ml) and water (60 ml) and was refluxed overnight. Water (150 ml) and diethyl ether were added and the organic layer was separated. To the organic layer was added a saturated sodium bicarbonate solution and the aqueous layer was separated. The aqueous layer was made acidic by additon of conc sulfuric acid. The acidic water solution was extracted with diethyl ether and the organic layer was washed with water, dried (Na2SO4) and evaporated under reduced pressure to give 6.5 g of the title compound.

후처리

  1. temperaturewas refluxed overnight
  2. customthe organic layer was separated
  3. additionTo the organic layer was added a saturated sodium bicarbonate solution
  4. customthe aqueous layer was separated
  5. extractionThe acidic water solution was extracted with diethyl ether
  6. washthe organic layer was washed with water
  7. dry with materialdried (Na2SO4)
  8. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-a531a3da22ea44cdbed049cffe203659
출처 데이터셋
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06790960B2

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