Choline, hydroxide → Methane

HRID 362679

반응식

HRID 362679 반응식
[C:1]([OH:22])(=[O:21])[CH2:2][CH2:3][CH2:4]/[CH:5]=[CH:6]\[CH2:7][CH:8]=[CH:9][CH2:10][CH:11]=[CH:12][CH2:13][CH:14]=[CH:15][CH2:16][CH:17]=[CH:18][CH2:19][CH3:20].[OH-].OCC[N+](C)(C)C>>[CH4:1].[C:1]([OH:22])(=[O:21])[CH2:2][CH2:3][CH2:4]/[CH:5]=[CH:6]\[CH2:7][CH:8]=[CH:9][CH2:10][CH:11]=[CH:12][CH2:13][CH:14]=[CH:15][CH2:16][CH:17]=[CH:18][CH2:19][CH3:20]

참가 물질

4

반응물 2

HCID 31255Choline, hydroxideHCID 70198906Npc164440

생성물 2

HCID 297MethaneHCID 70198906Npc164440

실험 절차

30.2 g of 5,8,11,14,17-cis-eicosapentaenoic acid (EPA, purity >90%) are treated with 12.1 of choline hydroxide according to one of the procedures described in examples 1 to 3. After charcoal treatment EPA choline salt is thus obtained with a nearly theoretical yield. The product is water-soiuble and its physicochemical and analytical characteristics conform to the expected values.

출처 및 근거

ORD 기록
ord-3e1f0079d11a496a987c23ce77ded36b
출처 데이터셋
uspto-grants-1999_02
특허 번호
US05869714

연결된 노트

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