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4-Methoxybenzoic Acid → HCID 68659330, 화합물

HRID 505446
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HRID 505446 반응식
C([Li])(CC)C.[C:6]([OH:16])(=[O:15])[C:7]1[CH:12]=CC(OC)=C[CH:8]=1.CN(CCN(C)C)C.[F:25][C:26]1[CH:27]=[C:28]([CH:34]=[CH:35][CH:36]=1)[C:29]([O:31]CC)=O.[CH2:37]1[CH2:41][O:40][CH2:39][CH2:38]1>>[F:25][C:26]1[CH:27]=[C:28]([CH:34]=[CH:35][CH:36]=1)[C:29]([C:8]1[CH:38]=[CH:37][C:41]([O:40][CH3:39])=[CH:12][C:7]=1[C:6]([OH:16])=[O:15])=[O:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 74784-Methoxybenzoic AcidHCID 8028TetrahydrofuranHCID 8037N,N,N',N'-TetramethylethylenediamineHCID 67975Benzoic acid, 3-fluoro-, ethyl esterHCID 178418400CID 53628100

생성물 1

HCID 68659330HCID 68659330, 화합물

실험 절차

s-Butyllithium (52 mL, 1.4 M in pentane, 72 mmol) was added at −78 C over 90 min. to a solution of p-Anisic acid (5 g, 33 mmol) and TMEDA (11 ml, 72 mmol) in THF (80 mL). After stirring for 15 min. ethyl 3-fluorobenzoate (5 mL, 40 mmol) was added in one portion. The reaction mixture was stirred for 15 min. then it was quenched with water (20 mL). The reaction mixture was then warmed to room temperature poured into water (1.5 L) 1N NaOH (30 ml) was added and the reaction mixture was then extracted with EtOAc. The extracts were discarded. The aqueous phase was then acidified with conc. HCl to pH 1 and extracted with EtOAc. Drying (Na2SO4) and concentration gave a residue which was recrystallized from hexanes/EtOAc to give the title compound as a white solid.

후처리

  1. additionwas added in one portion
  2. customit was quenched with water (20 mL)
  3. additionpoured into water (1.5 L) 1N NaOH (30 ml)
  4. additionwas added
  5. extractionthe reaction mixture was then extracted with EtOAc
  6. extractionextracted with EtOAc
  7. customDrying
  8. concentration(Na2SO4) and concentration
  9. customgave a residue which
  10. customwas recrystallized from hexanes/EtOAc

출처 및 근거

ORD 기록
ord-1764eb1921964e0188df4702d06cc015
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07781457B2

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