Adipic Acid → 1,2,3-Propanetricarboxylic acid

HRID 926344

反応式

HRID 926344 の反応式
[C:1]([OH:10])(=O)[CH2:2][CH2:3]CC[C:6]([OH:8])=[O:7].[C:11]([OH:22])(=[O:21])[CH2:12][CH:13]([CH2:17][C:18]([OH:20])=[O:19])[C:14]([OH:16])=[O:15].C(C(O)=O)C(C(O)=O)C(C(O)=O)CC(O)=O.C1C(C2OC2)CC2OC2C1>>[C:6](=[O:8])=[O:7].[CH2:1]1[O:10][CH:2]1[CH3:3].[C:11]([OH:22])(=[O:21])[CH2:12][CH:13]([CH2:17][C:18]([OH:20])=[O:19])[C:14]([OH:16])=[O:15]

参加物

6

反応物 4

HCID 196Adipic AcidHCID 7833Vinyl cyclohexene dioxideHCID 149251,2,3-Propanetricarboxylic acidHCID 155601,2,3,4-Butanetetracarboxylic acid

生成物 2

HCID 149251,2,3-Propanetricarboxylic acidHCID 18518868Carbon dioxide propylene oxide

実験手順

After fixing a chain transfer agent to control a molar fraction of —COOH group to 45 relative to a molar fraction of the catalyst and then introducing adipic acid, 5.9 mg (Entries 1 to 5); tricarballylic acid, 5.1 mg (Entries 6 to 10); 1,2,3,4-butane tetracarboxylic acid, 4.7 mg (Entries 11 to 15)) into a reactor, vinylcyclohexene dioxide was weighed to numeral values listed in TABLE 3, relative to the molar fraction of the catalyst and then introduced (into the reactor). Then, polymerization was executed and the catalyst was removed according to the same procedures as described in Example 1, resulting in pure copolymer. TABLE 3 summarizes results of the polymerization. FIG. 2 shows GPC curves of a copolymer obtained by carbon dioxide/propylene oxide copolymerization in the presence of tricarballylic acid (C3H5(CO2H)3) and diepoxide, wherein reference numeral in each curve denotes an entry number in TABLE 2.

後処理

  1. additionintroduced (into the reactor)
  2. customThen, polymerization
  3. customthe catalyst was removed
  4. customresulting in pure copolymer
  5. customTABLE 3 summarizes results of the polymerization

出典と根拠

ORDレコード
ord-49e07011850448748199983a8c14f118
出典データセット
uspto-grants-2016_03
特許番号
US09284407B2

関連ノート

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