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Toluene → Methyl 3-amino-5-fluorobenzoate

HRID 595993
ノート
印刷プレビュー

反応式

HRID 595993 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 3807862Methyl 3-amino-5-fluorobenzoate

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-becedcce27044c5bae184bbd4de05046
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242996B2

反応ノート

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