Chloride → 2,5-Dimethyl-3,6-dihexyl-pyrazine

HRID 1606190

반응식

HRID 1606190 반응식
[N:1](=[C:3]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[C:4](=O)[CH3:5])O.[CH3:13][C:14](=O)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21].[Cl-].[NH:24]=C=O>[Zn].C(O)(=O)C>[CH3:13][C:14]1[C:15]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])=[N:24][C:4]([CH3:5])=[C:3]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:1]=1

참가 물질

7

반응물 4

HCID 312ChlorideHCID 6347Isocyanic acidHCID 131872-NonanoneHCID 736826343-Oximino-2-nonanone

생성물 1

HCID 218149392,5-Dimethyl-3,6-dihexyl-pyrazine

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

5h. 2,5-Dimethyl-3,6-dihexyl-pyrazine was prepared by first forming 3-oximino-2-nonanone by reacting 2-nonanone with nitrocyl chloride according to the method of BOUVEAULT (loc.cit.). The autocondensation of two moles of the imino-ketone in the presence of zinc and acetic acid [according to the method described in Chimia 11, 310 (1957)] yielded 2,5-dimethyl-3,6-dihexyl-pyrazine which had a b.p. of 112°-120°C./0.01 mm. Hg.

후처리

  1. custom5h

출처 및 근거

ORD 기록
ord-34a45f4a20f24b4fb421621f1435b259
출처 데이터셋
uspto-grants-1976_04
특허 번호
US03952024

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