Phenolphthalein → HCID 20071852, 화합물

HRID 981319노트

반응식

HRID 981319 반응식
[OH-].[CH2:2]([N+:8]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].C1C=[C:31]2[C:33]([O:35]C(C3C=CC(O)=CC=3)(C3C=CC(O)=CC=3)[C:30]2=CC=1)=[O:34].C(O)(=O)C=C>CO>[C:33]([O-:35])(=[O:34])[CH:31]=[CH2:30].[CH2:21]([N+:8]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7])([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]

참가 물질

5

반응물 3

HCID 4764PhenolphthaleinHCID 6581Acrylic AcidHCID 13998878N,N,N-Trihexylhexan-1-aminium hydroxide

생성물 1

HCID 20071852HCID 20071852, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

The AgOH is resuspended in 400 ml of methanol. The purified tetraalkylammonium iodide (0.1 moles or 48.2 g) (Aldrich Chemical Co., Milwaukee, Wis.) is dissolved separately in 100 ml. of methanol and added to the AgOH suspension. Almost immediately, the AgOh develops a greenish cast. The mixture is stirred for an hour and then filtered through a sintered-glass funnel. The filtrate now contains 0.1 moles of tetrahexylammonium hydroxide. A small amount of phenophthalein is added, turning the solution red indicating that the solution is basic. Acrylic acid is added until the red color disappears. The methanol is removed by evaporation in a rotary flash evaporator leaving tetrahexylammonium acrylate. The resulting tetrahexylammonium acrylate was found to be electrically conductive.

후처리

  1. filtrationfiltered through a sintered-glass funnel
  2. customThe methanol is removed by evaporation in a rotary flash evaporator

출처 및 근거

ORD 기록
ord-69b7dfbbe8974a56aa2679fdc9975f7c
출처 데이터셋
uspto-grants-1991_02
특허 번호
US04990581

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