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Toluene → Methyl 3-amino-5-fluorobenzoate

HRID 595993
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HRID 595993 반응식
BrC1[CH:3]=[C:4]([CH:8]=[C:9]([F:11])[CH:10]=1)[C:5]([OH:7])=[O:6].[C:12]1(C)C=CC=CC=1.[Si]([CH:23]=[N+:24]=[N-])(C)(C)C>CO>[NH2:24][C:23]1[CH:3]=[C:4]([CH:8]=[C:9]([F:11])[CH:10]=1)[C:5]([O:7][CH3:12])=[O:6]
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참가 물질

5

반응물 3

HCID 1140TolueneHCID 167693TrimethylsilyldiazomethaneHCID 27733393-Bromo-5-fluorobenzoic acid

생성물 1

HCID 3807862Methyl 3-amino-5-fluorobenzoate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

3-bromo-5-fluorobenzoic acid (6.12 g, 33.1 mmol) was dissolved in MeOH (10 mL) and cooled in ice-water bath and toluene (50 mL) and then TMS-diazomethane (19.84 mL, 39.7 mmol) was added dropwise. Reaction mixture was allowed to return to room temperature for 1 h and concentrated in vacuo and the residue dissolved in DCM/Ether and filtered through a short plug of silica and the filtrate evaporated in vacuo to afford the desired product which was then dissolved in MeOH (60 mL) and Pd/C 10 wt % 3.3 g was added and the mixture evacuated and stirred under 1 atm of hydrogen overnight and LCMS indicated desired product next morning. The reaction mixture was filtered through Celite and the filtrate was concnetrated in vacuo and the residue azeotroped with toluene twice and taken to the next step as such (99%). LCMS (m/z): 211.1 (MH+), 0.55 min.

후처리

  1. customReaction mixture
  2. concentrationconcentrated in vacuo
  3. dissolutionthe residue dissolved in DCM/Ether
  4. filtrationfiltered through a short plug of silica
  5. customthe filtrate evaporated in vacuo

출처 및 근거

ORD 기록
ord-becedcce27044c5bae184bbd4de05046
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242996B2

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