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Water → 3,4-Dihydroxy-5-(trifluoromethyl)benzoic acid

HRID 62779
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HRID 62779 반응식
B(Br)(Br)Br.[OH:5][C:6]1[C:14]([C:15]([F:18])([F:17])[F:16])=[CH:13][C:9]([C:10]([OH:12])=[O:11])=[CH:8][C:7]=1[O:19]C.O>C(Cl)Cl>[OH:19][C:7]1[CH:8]=[C:9]([CH:13]=[C:14]([C:15]([F:16])([F:17])[F:18])[C:6]=1[OH:5])[C:10]([OH:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 670417934-Hydroxy-3-methoxy-5-(trifluoromethyl)benzoic acid

생성물 1

HCID 670415763,4-Dihydroxy-5-(trifluoromethyl)benzoic acid수율 69.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Boron tribromide (392 μL, 4.15 mmol) was added to a suspension of 4-hydroxy-3-methoxy-5-(trifluoromethyl)benzoic acid (4) (392 mg, 1.66 mmol) in DCM (10 mL) at 0° C. The reaction mixture was allowed to warm to RT and stirred for 70 h. The reaction mixture was cautiously added to stirring iced water (50 mL) and stirred for 10 min. The product was extracted with DCM (2×20 mL), and then the combined organic extracts were washed with brine (2×20 mL). The solvent was removed in vacuo and the residue was purified by silica chromatography (12 g, 0-10% MeOH in DCM) to afford 3,4-dihydroxy-5-(trifluoromethyl)benzoic acid (5) (257 mg, 68%) as a white solid: m/z 221 [M−H]− (ES−); 1H NMR (400 MHz, DMSO-d6) δ: 12.83 (1H, br s), 10.45 (2H, br d), 7.56 (2H, dd).

후처리

  1. additionThe reaction mixture was cautiously added
  2. stirringstirred for 10 min
  3. extractionThe product was extracted with DCM (2×20 mL)
  4. washthe combined organic extracts were washed with brine (2×20 mL)
  5. customThe solvent was removed in vacuo
  6. customthe residue was purified by silica chromatography (12 g, 0-10% MeOH in DCM)

출처 및 근거

ORD 기록
ord-7c55e024cf3b4a908a798dae98515257
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447028B2

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