Sodium Hydroxide → 2-O-(5-Methyl-3-isoxazolyl)glycerol

HRID 974688

反応式

HRID 974688 の反応式
[CH3:1][C:2]1[O:6][N:5]=[C:4]([O:7][CH:8]([C:14](OCC)=[O:15])[C:9](OCC)=[O:10])[CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+]>O1CCCC1>[CH3:1][C:2]1[O:6][N:5]=[C:4]([O:7][CH:8]([CH2:14][OH:15])[CH2:9][OH:10])[CH:3]=1

参加物

5

反応物 3

HCID 14798Sodium HydroxideHCID 19986058Diethyl 2-(5-methyl-3-isoxazolyloxy)malonateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 543308062-O-(5-Methyl-3-isoxazolyl)glycerol収率 70.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 23.72 g of diethyl 2-(5-methyl-3-isoxazolyloxy)malonate (prepared as described in Preparation 19) in 120 ml of tetrahydrofuran was added dropwise to a suspension of 14.00 g of lithium aluminum hydride in 140 ml of tetrahydrofuran over a period of 30 minutes, whilst ice-cooling. The mixture was stirred at room temperature for 40 hours, after which 56 ml of a 4% w/v aqueous solution of sodium hydroxide was added dropwise to it over a period of 30 minutes, whilst ice-cooling. An insoluble material was filtered off using a Celite (trade mark) filter aid, and the filtrate was concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through 300 g of silica gel. 11.26 g of the title compound was isolated as a colorless oil from the fractions eluted with ethyl acetate.

後処理

  1. temperaturecooling
  2. temperaturecooling
  3. filtrationAn insoluble material was filtered off
  4. filtrationfilter aid
  5. concentrationthe filtrate was concentrated by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-d0633e3606254a05ad8c7ee4d665fd87
出典データセット
uspto-grants-1991_11
特許番号
US05068340

関連ノート

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