Sodium borohydride → [1-(Benzyloxy)-2-naphthyl]methanol

HRID 433149ノート

反応式

HRID 433149 の反応式
[CH2:1]([O:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][C:10]=1[CH:19]=[O:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>CO>[CH2:1]([O:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][C:10]=1[CH2:19][OH:20])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 156178221-(Benzyloxy)-2-naphthaldehyde

生成物 1

HCID 23431826[1-(Benzyloxy)-2-naphthyl]methanol収率 99%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 1-(benzyloxy)-2-naphthaldehyde (7.00 g, 26.7 mmol) in methanol (250 mL) at 0° C. was added sodium borohydride (1.51 g, 40.0 mmol) and the reaction mixture was allowed to stir at room temperature for 24 h. The solvent was removed in vacuo to give a crude solid which was partitioned between ethyl acetate (300 mL) and water (300 mL). The organic layer was separated and washed with water (300 mL), aqueous sodium chloride (300 mL), dried (magnesium sulfate) and filtered through a plug of silica (10 cm×5 cm). The solvent was removed in vacuo to give 6.98 g (99%) of [1-(benzyloxy)-2-naphthyl]methanol as white crystalline solid. Rf=0.36 (silica, dichloromethane:hexanes 3:2); mp 85-87° C. Anal. Calcd. for C18H16O2: C, 81.24; H, 6.14. Found: C, 81.03; H, 5.98.

後処理

  1. customThe solvent was removed in vacuo
  2. customto give a crude solid which
  3. customwas partitioned between ethyl acetate (300 mL) and water (300 mL)
  4. customThe organic layer was separated
  5. washwashed with water (300 mL), aqueous sodium chloride (300 mL)
  6. dry with materialdried (magnesium sulfate)
  7. filtrationfiltered through a plug of silica (10 cm×5 cm)
  8. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-d61f9339ea9642b3b576f5eac92c9754
出典データセット
uspto-grants-2003_12
特許番号
US06667322B2

反応ノート

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