Hydrochloric Acid → 2,3-Dihydro-6-hydroxy-7-methoxy-5-benzofurancarboxaldehyde

HRID 2419544

反応式

HRID 2419544 の反応式
[CH3:1][O:2][C:3]1[C:11]2[O:10][CH2:9][CH2:8][C:7]=2[CH:6]=[CH:5][C:4]=1[OH:12].Cl.C[CH2:15][O:16]CC>[C-]#N.[Zn+2].[C-]#N>[OH:12][C:4]1[C:5]([CH:15]=[O:16])=[CH:6][C:7]2[CH2:8][CH2:9][O:10][C:11]=2[C:3]=1[O:2][CH3:1]

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 218565712,3-Dihydro-7-methoxy-6-benzofuranol

生成物 1

HCID 218565722,3-Dihydro-6-hydroxy-7-methoxy-5-benzofurancarboxaldehyde

試薬・触媒・溶媒 1

HCID 11186Zinc cyanide (Zn(CN)2)触媒

実験手順

A mixture of 2.49 g. (15 mmole) of 2.3-Dihydro-7-methoxy-6-benzofuranol, 5.87 g. (50 mmole) zinc cyanide and 100 ml. of dry ether was saturated with hydrogen chloride for 1 hour at 0°, then for 2 hours at room temperature. The mixture was then allowed to stand overnight at room temperature then concentrated in vacuo and the residue treated with 100 ml. of 0.1N HCl for 1 hour at reflux. After cooling, ether extraction provided the product which was purified by chromatography over silica gel (E. Merck 60), eluting with CHCl3, to yield a colorless solid, m.p. 71°-72°.

後処理

  1. additionA mixture of 2.49 g
  2. waitto stand overnight at room temperature
  3. concentrationthen concentrated in vacuo
  4. additionthe residue treated with 100 ml
  5. temperatureof 0.1N HCl for 1 hour at reflux
  6. temperatureAfter cooling
  7. extractionether extraction
  8. customprovided the product which
  9. customwas purified by chromatography over silica gel (E. Merck 60)
  10. washeluting with CHCl3
  11. customto yield a colorless solid, m.p. 71°-72°

出典と根拠

ORDレコード
ord-c06526962ddc4d3d9083bee231100b09
出典データセット
uspto-grants-1978_08
特許番号
US04107182

関連ノート

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