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Acetic Acid → 5,6,7-Trimethyl-2,3-dihydro-1-benzofuran

HRID 1980800
ノート
印刷プレビュー

反応式

HRID 1980800 の反応式
Cl.[CH3:2][C:3]1[C:4]([CH:13]=O)=[CH:5][C:6]2[CH2:10][CH2:9][O:8][C:7]=2[C:11]=1[CH3:12].C(O)(=O)C>[Zn].O>[CH3:13][C:4]1[C:3]([CH3:2])=[C:11]([CH3:12])[C:7]2[O:8][CH2:9][CH2:10][C:6]=2[CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 176Acetic AcidHCID 313Hydrochloric Acid2 回HCID 204005066,7-Dimethyl-2,3-dihydro-1-benzofuran-5-carbaldehyde

生成物 1

HCID 204004915,6,7-Trimethyl-2,3-dihydro-1-benzofuran収率 79%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 962Water溶媒
3 回

実験手順

Zinc amalgum [prepared by heating a mixture of zinc dust (7.0 g), mercuric chloride (0.70 g), concentrated hydrochloric acid (0.5 ml) and water (30 ml) for 5 minutes and then decanting the aqueous solution] was added to a mixture of 2,3-dihydro-6,7-dimethylbenzo[b]furan-5-carboxaldehyde (6.93 g, 39 mmol), acetic acid (50 ml), water (50 ml), and concentrated hydrochloric acid (100 ml). The mixture was heated at reflux with vigorous stirring for 12 hours. After cooling, the mixture was poured into water. The dried (Na2SO4) ether extract was evaporated and the residue was purified by column chromatography over silica with hexane elution to give 2,3-dihydro-5,6,7-trimethylbenzo[b]furan (5.00 g, 78%) as a white solid, mp <50° C.

後処理

  1. temperatureby heating
  2. customdecanting the aqueous solution]
  3. temperatureThe mixture was heated
  4. temperatureat reflux
  5. temperatureAfter cooling
  6. dry with materialThe dried (Na2SO4) ether
  7. extractionextract
  8. customwas evaporated
  9. customthe residue was purified by column chromatography over silica with hexane elution

出典と根拠

ORDレコード
ord-5a70604997a348ff964c61158d2a5fc8
出典データセット
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04511391

反応ノート

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