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Water → 4-Fluorobenzo[b]thiophene

HRID 2173026
ノート
印刷プレビュー

反応式

HRID 2173026 の反応式
[F:1][C:2]1[C:10]2[CH:9]=[C:8](C(O)=O)[S:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.N12CCCN=C1CCCCC2.O>CC(N(C)C)=O>[F:1][C:2]1[C:10]2[CH:9]=[CH:8][S:7][C:6]=2[CH:5]=[CH:4][CH:3]=1
参加物反応条件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 962WaterHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 7378554-Fluoro-1-benzothiophene-2-carboxylic acid

生成物 1

HCID 190880174-Fluorobenzo[b]thiophene

試薬・触媒・溶媒 1

HCID 31374Dimethylacetamide溶媒

反応条件

温度
200 °C

実験手順

A mixture of 4-fluorobenzo[b]thiophene-2-carboxylic acid (200 mg, 1.019 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.457 mL, 3.06 mmol) in DMA (1 mL) was heated at 200° C. for 1 hour. The reaction mixture was allowed to cool and was poured into water (100 mL). The product was extracted with hexane (2×20 mL) and washed with 1N HCl (100 mL) and 1N NaOH (50 mL). The organic layers were combined, dried over Na2SO4 and the solvent was removed in vacuo to give the title compound as a yellow oil, which was used without further purification.

後処理

  1. temperatureto cool
  2. extractionThe product was extracted with hexane (2×20 mL)
  3. washwashed with 1N HCl (100 mL) and 1N NaOH (50 mL)
  4. dry with materialdried over Na2SO4
  5. customthe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-2598a0fc07214e719019d641221fc41a
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09056873B2

反応ノート

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