Oxonium, triethyl-, hexafluorophosphate(1-) (1:1) → 5-Bromo-thiophene 2-carboximidic acid ethyl ester

HRID 1020952ノート

反応式

HRID 1020952 の反応式
[Br:1][C:2]1[S:6][C:5]([C:7]([NH2:9])=[O:8])=[CH:4][CH:3]=1.F[P-](F)(F)(F)(F)F.[CH2:17]([O+](CC)CC)[CH3:18]>ClC(Cl)C>[CH2:17]([O:8][C:7]([C:5]1[S:6][C:2]([Br:1])=[CH:3][CH:4]=1)=[NH:9])[CH3:18]

参加物

4

反応物 2

HCID 167684Oxonium, triethyl-, hexafluorophosphate(1-) (1:1)HCID 6057225-Bromothiophene-2-carboxamide

生成物 1

HCID 583718665-Bromo-thiophene 2-carboximidic acid ethyl ester

試薬・触媒・溶媒 1

HCID 63651,1-Dichloroethane溶媒

反応条件

温度
90 °C

実験手順

The 5-bromo-thiophene 2-carboxylic acid amide (2BW) (7 g, 34.1 mmols) was dissolved in dichloroethane (170 ml). Triethyloxonium hexafluorophosphate (10.16 g, 40.97 mmols) was added and the resulting mixture was refluxed for 1 hr at 90° C. The reaction mixture was concentrated under reduced pressure, and was taken directly to next step.

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-b62ef39db1c84eb1bdb70fd3c47d91c8
出典データセット
uspto-grants-2014_05
特許番号
US08716483B2

反応ノート

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