N-(4-Hydroxyphenyl)Phthalimide → Methyl 7-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenoxy]-2,2-dimethylheptanoate

HRID 648987ノート

反応式

HRID 648987 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:12](=[O:13])[C:11]3=[CH:14][CH:15]=[CH:16][CH:17]=[C:10]3[C:9]2=[O:18])=[CH:4][CH:3]=1.O(C)[Na].[CH3:22][C:23]([CH3:34])([CH2:28][CH2:29][CH2:30][CH2:31][CH2:32]I)[C:24]([O:26][CH3:27])=[O:25]>CN(C=O)C>[O:18]=[C:9]1[C:10]2[C:11](=[CH:14][CH:15]=[CH:16][CH:17]=2)[C:12](=[O:13])[N:8]1[C:5]1[CH:4]=[CH:3][C:2]([O:1][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][C:23]([CH3:22])([CH3:34])[C:24]([O:26][CH3:27])=[O:25])=[CH:7][CH:6]=1

参加物

5

実験手順

N-[p-Hydroxyphenyl]phthalimide (5.0 g) described in Example 1 was dissolved in 100 ml of DMF and 1.13 g of NaOCH3 was added. The solution was stirred at room temperature for one-half hour, then 6.25 g of methyl 2,2-dimethyl-7-iodoheptanoate was added dropwise. The mixture was stirred at room temperature overnight and then heated at reflux for two hours and concentrated on rotary evaporator. H2O (100 ml) was added and a solid was obtained. The product was extracted with EtOAc leaving the insoluble starting material behind. Concentration of the ethyl acetate solution followed by recrystallization of the resulting solid from isopropyl ether gave the purified product; mp 82°-3° C.

後処理

  1. stirringThe mixture was stirred at room temperature overnight
  2. temperatureheated
  3. temperatureat reflux for two hours
  4. concentrationconcentrated on rotary evaporator
  5. additionH2O (100 ml) was added
  6. customa solid was obtained
  7. extractionThe product was extracted with EtOAc leaving the
  8. customConcentration of the ethyl acetate solution followed by recrystallization of the resulting solid from isopropyl ether
  9. customgave the purified product

出典と根拠

ORDレコード
ord-ecc46022bff34e7b893d5c141d74ad87
出典データセット
uspto-grants-1988_04
特許番号
US04737512

反応ノート

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