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Water → HCID 20213775, 화합물

HRID 1906032
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HRID 1906032 반응식
[OH:1][C:2]1[CH:23]=[C:22]([OH:24])[CH:21]=[CH:20][C:3]=1[C:4]([CH2:6][CH2:7][CH2:8][CH2:9][C:10](=[O:19])[C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][C:12]=1[OH:18])=[O:5].[CH2:25]([CH:27]1[O:29][CH2:28]1)Cl.[OH-:30].[Na+].[OH2:32]>[Cl-].C[N+](C)(C)C>[CH2:25]([O:1][C:2]1[CH:23]=[C:22]([O:24][CH2:25][CH:27]2[O:29][CH2:28]2)[CH:21]=[CH:20][C:3]=1[C:4]([CH2:6][CH2:7][CH2:8][CH2:9][C:10](=[O:19])[C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:3][CH:2]2[O:30][CH2:23]2)=[CH:13][C:12]=1[O:18][CH2:4][CH:6]1[O:32][CH2:7]1)=[O:5])[CH:27]1[O:29][CH2:28]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water3회HCID 7835EpichlorohydrinHCID 14798Sodium HydroxideHCID 283375Hexane-1,6-dione, 1,6-bis(2,4-dihydroxyphenyl)-

생성물 1

HCID 20213775HCID 20213775, 화합물

시약·촉매·용매 1

HCID 6379Tetramethylammonium chloride촉매

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온도
60 °C

실험 절차

18.16 g (0.055 mole) of 1,4-bis-(2',4'-dihydroxybenzoyl)-butane, 86.84 g (0.938 mole) of epichlorohydrin and 0.97 g of 50% aqueous tetramethylammonium chloride solution are initially placed in a 350 ml sulfonation flask equipped with a stirrer, a thermometer, a condenser, a dropping funnel and a water separator, and are heated at 105°-110° C. After a reaction time of 4 hours the reaction mixture is cooled to 60° C.; 20.21 g (0.253 mole) of 50% aqueous sodium hydroxide solution are then added with simultaneous removal of water from the system. The resulting suspension is treated with water, and the organic phase is washed with water, dried over sodium sulphate and concentrated. This gives 28.62 g (93.84% of theory) of a red, viscous resin.

후처리

  1. customequipped with a stirrer
  2. washthe organic phase is washed with water
  3. dry with materialdried over sodium sulphate
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9008c956e24f4443874f47cd15f0a104
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04649181

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