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Boron tribromide → 5-(3-amino-2-hydroxy-phenyl)-1,2,4-trimethyl-1H-pyrrole-3-carboxylic acid ethyl ester hydrobromide

HRID 384306
ノート
印刷プレビュー

反応式

HRID 384306 の反応式
[CH2:1]([O:3][C:4]([C:6]1[C:10]([CH3:11])=[C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([NH2:18])[C:13]=2[O:19]C)[N:8]([CH3:21])[C:7]=1[CH3:22])=[O:5])[CH3:2].B(Br)(Br)[Br:24]>ClCCl>[BrH:24].[CH2:1]([O:3][C:4]([C:6]1[C:10]([CH3:11])=[C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([NH2:18])[C:13]=2[OH:19])[N:8]([CH3:21])[C:7]=1[CH3:22])=[O:5])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 25134Boron tribromideHCID 596156885-(3-amino-2-methoxy-phenyl)-1,2,4-trimethyl-1H-pyrrole-3-carboxylic acid ethyl ester

生成物 1

HCID 686128175-(3-amino-2-hydroxy-phenyl)-1,2,4-trimethyl-1H-pyrrole-3-carboxylic acid ethyl ester hydrobromide収率 82.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

5-(3-Amino-2-methoxy-phenyl)-1,2,4-trimethyl-1H-pyrrole-3-carboxylic acid ethyl ester 6g (210 mg, 0.69 mmol) was dissolved in 5 mL of dichloromethane followed by addition of boron tribromide (1.39 mL, 2.78 mmol). The reaction mixture was reacted at room temperature for 0.5 hours and monitored by TLC until the disappearance of the starting materials. The reaction was quenched with methanol, and the mixture was concentrated under reduced pressure followed by addition of 50 mL of ethyl acetate and 15 mL of saturated aqueous sodium bicarbonate. The mixture was mixed well and the layers were separated. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, filtered to remove the drying agent and concentrated under reduced pressure to obtain the title compound 5-(3-amino-2-hydroxy-phenyl)-1,2,4-trimethyl-1H-pyrrole-3-carboxylic acid ethyl ester hydrobromide 6h (165 mg, yield 82.5%) as a white solid.

後処理

  1. customThe reaction mixture was reacted at room temperature for 0.5 hours
  2. customThe reaction was quenched with methanol
  3. concentrationthe mixture was concentrated under reduced pressure
  4. additionfollowed by addition of 50 mL of ethyl acetate and 15 mL of saturated aqueous sodium bicarbonate
  5. additionThe mixture was mixed well
  6. customthe layers were separated
  7. washThe organic layer was washed with saturated brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. customto remove the drying agent
  11. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-5810ade36a3a42b681c92b317d90040c
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08367710B2

反応ノート

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