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4-Methoxybenzyl alcohol → 4-((4-Methoxybenzyl)oxy)-2-methylene-4-oxobutanoic acid

HRID 2165338
ノート
印刷プレビュー

反応式

HRID 2165338 の反応式
[C:1]1(=[O:8])[O:7][C:5](=[O:6])[CH2:4][C:2]1=[CH2:3].[CH3:9][O:10][C:11]1[CH:18]=[CH:17][C:14]([CH2:15][OH:16])=[CH:13][CH:12]=1>CCCCCC>[CH3:9][O:10][C:11]1[CH:18]=[CH:17][C:14]([CH2:15][O:16][C:5]([CH2:4][C:2]([C:1]([OH:8])=[O:7])=[CH2:3])=[O:6])=[CH:13][CH:12]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 77384-Methoxybenzyl alcoholHCID 75110Itaconic Anhydride

生成物 1

HCID 15126774-((4-Methoxybenzyl)oxy)-2-methylene-4-oxobutanoic acid収率 61%

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

A 250 ml one-necked round bottomed flask equipped with reflux condenser, nitrogen inlet, and magnetic stir bar was charged with itaconic anhydride (33.6 g, 0.3 mol) toluene (100 ml) and 4-methoxybenzyl alcohol (41.5 g, 0.3 mol). The solution was then warmed to reflux for 60 minutes and then cooled to room temperature. The solution was poured into a 500 ml Erlenmeyer flask, diluted with 100 ml of hexane and allowed to stand whereupon crystals of pure monoester formed. The product was isolated by filtration on a Buchner funnel and air dried to give 45.4 g, 61% of material with mp 83°-85° C., a second crop, 12.9 g, 17% was isolated after cooling of the filtrate in an ice bath.

後処理

  1. customA 250 ml one-necked round bottomed flask equipped
  2. temperaturewith reflux condenser, nitrogen inlet, and magnetic stir bar
  3. temperatureThe solution was then warmed
  4. temperatureto reflux for 60 minutes
  5. additionThe solution was poured into a 500 ml Erlenmeyer flask
  6. customformed
  7. customThe product was isolated by filtration on a Buchner funnel and air
  8. customdried

出典と根拠

ORDレコード
ord-e55f0a0671fd4759a2b868d4d9a5a9d7
出典データセット
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04939288

反応ノート

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