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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Boron trifluoride etherate → Methyl 3-fluoro-2-methylbenzoate

HRID 1261497
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HRID 1261497 반응식
[F:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].B(F)(F)F.[CH3:16]COCC>CO>[CH3:16][O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][CH:10]=[C:2]([F:1])[C:3]=1[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8000Boron trifluoride etherateHCID 2466823-Fluoro-2-methylbenzoic acid

생성물 1

HCID 21752566Methyl 3-fluoro-2-methylbenzoate수율 87%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 3-fluoro-2-methyl-benzoic acid (Aldrich, 10.2 g, 66.17 mmol) in methanol (135 mL) at room temperature was treated with boron trifluoride etherate (15 mL) and was allowed to stir at room temperature. The reaction mixture was then concentrated in vacuo to remove the methanol and then diethyl ether (˜300 mL) was added. The solution was transferred to a separatory funnel and washed with water (200 mL) and a 5% aqueous sodium bicarbonate solution to pH>7.5. The organic layer was then dried over magnesium sulfate and concentrated in vacuo to afford 3-fluoro-2-methyl-benzoic acid methyl ester (9.74 g, 87%) as a light orange colored oil which was used without purification.

후처리

  1. concentrationThe reaction mixture was then concentrated in vacuo
  2. customto remove the methanol
  3. additiondiethyl ether (˜300 mL) was added
  4. customThe solution was transferred to a separatory funnel
  5. washwashed with water (200 mL)
  6. dry with materialThe organic layer was then dried over magnesium sulfate
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-b1b703bc45074664a0a5817441bdb59e
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08470866B2

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