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Hydrochloric Acid → 1-Phenyl-3-buten-2-one

HRID 2294951
ノート
印刷プレビュー

反応式

HRID 2294951 の反応式
[CH:1]([Mg]Br)=[CH2:2].CON(C)[C:8](=[O:16])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.Cl>O1CCCC1>[C:10]1([CH2:9][C:8](=[O:16])[CH:1]=[CH2:2])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
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 313Hydrochloric AcidHCID 10419762N-Methoxy-N-methyl-2-phenylacetamideHCID 178418507HCID 178418507、化合物

生成物 1

HCID 377341-Phenyl-3-buten-2-one収率 73%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A 1M solution of vinylmagnesium bromide in THF (80 mL, 80 mmol) was added dropwise to a stirred solution of N-methoxy-N-methylphenylacetamide (12.8 g, 71.5 mmol) in distilled tetrahydrofuran (THF) (200 mL), cooled to 0°-5° C. in an ice-water bath. The solution was stirred at 0°-5° C. for 2 h and was then poured into cold 1N HCl solution (150 mL). The THF layer was separated and the aqueous (aq.) layer was extracted with EtOAc (100 mL). Organic extracts were combined, dried (MgSO4), filtered and concentrated. The crude oil was chromatographed on a silica gel column and eluted with 5-20% ethylacetate (EtOAc) in hexanes to obtain title 4-phenyl-but-1-ene-3-one (7.62 g, 73%) as an oil.

後処理

  1. temperaturecooled to 0°-5° C. in an ice-water bath
  2. customThe THF layer was separated
  3. extractionthe aqueous (aq.) layer was extracted with EtOAc (100 mL)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude oil was chromatographed on a silica gel column
  8. washeluted with 5-20% ethylacetate (EtOAc) in hexanes

出典と根拠

ORDレコード
ord-fe12891b8b7a4109899edadd3de55e0a
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05691356

反応ノート

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