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

HRID 2165338
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HRID 2165338 반응식
[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
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참가 물질

4

반응물 2

HCID 77384-Methoxybenzyl alcoholHCID 75110Itaconic Anhydride

생성물 1

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

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-e55f0a0671fd4759a2b868d4d9a5a9d7
출처 데이터셋
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04939288

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