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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Formylbenzoic acid → HCID 59811331, 화합물

HRID 2113635
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HRID 2113635 반응식
[C:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)([OH:3])=[O:2].[CH2:12]([Mg]Cl)[C:13]([CH3:16])([CH3:15])[CH3:14]>C1COCC1.CCCCCC>[CH3:12][C:13]([CH3:16])([CH3:15])/[CH:14]=[CH:8]/[C:7]1[CH:10]=[CH:11][C:4]([C:1]([OH:3])=[O:2])=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 120884-Formylbenzoic acidHCID 178418809HCID 178418809, 화합물

생성물 1

HCID 59811331HCID 59811331, 화합물

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8058Hexane용매

실험 절차

To a cooled (0° C.) and well stirred suspension of 4-carboxy benzaldehyde (2.0 g, 13.32 mmol) in anhydrous THF (90 mL) is added 33.3 mmol of neopentyl magnesium chloride in hexane during 20 minutes and the mixture is stirred at the same temperature for an additional two hours before being quenched with satyrated ammonium chloride solution. Most of the THF is evaporated and the aqueous mixture is treated with conc. HCl (50 mL) and the mixture is heated to reflux for 2 hours. The mixture is then cooled to ambient temperature and extracted with methylene chloride (2×100 mL), the organic layer is dried over sodium sulfate and concentrated to obtain the desired 4-(3,3-dimethyl-but-1-enyl)-benzoic acid.

후처리

  1. temperatureTo a cooled
  2. custombefore being quenched with satyrated ammonium chloride solution
  3. customMost of the THF is evaporated
  4. additionthe aqueous mixture is treated with conc. HCl (50 mL)
  5. temperaturethe mixture is heated
  6. temperatureto reflux for 2 hours
  7. extractionextracted with methylene chloride (2×100 mL)
  8. dry with materialthe organic layer is dried over sodium sulfate
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-5e3a67fe2e2b4ebd808f0de389894432
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07432281B2

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