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Triethylamine → HCID 23462043, 화합물

HRID 2286700
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HRID 2286700 반응식
[OH:1][CH2:2][C:3]1[CH:8]=[N:7][C:6]([CH3:9])=[CH:5][N:4]=1.C(N(CC)CC)C.[C:17](Cl)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]>C1C=CC=CC=1>[C:17]([O:1][CH2:2][C:3]1[CH:8]=[N:7][C:6]([CH3:9])=[CH:5][N:4]=1)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 62493Pivaloyl chlorideHCID 5800615-Methyl-2-pyrazinemethanol

생성물 1

HCID 23462043HCID 23462043, 화합물수율 71.5%

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

To a solution of 2-hydroxymethyl-5-methylpyrazine (6.2 g) and triethylamine (6.4 ml) in anhydrous benzene (150 ml) dropwise addition was made of a solution of pivaloyl chloride (6.15 ml) in anhydrous benzene (50 ml). The solution was maintained at boiling for 7 hours, the solvent was then evaporated and the residue treated with acetone. After filtration of the insoluble solid, the filtrate was evaporated to dryness and the residue re-dissolved in chloroform. The chloroform solution was first dehydrated and then evaporated to dryness, obtaining 7 g (71.5%) of 5-methyl-2-pyrazinylmethyl pivalate, b.p.=74° C./0.1 mmHg.

후처리

  1. temperatureThe solution was maintained
  2. customthe solvent was then evaporated
  3. additionthe residue treated with acetone
  4. filtrationAfter filtration of the insoluble solid
  5. customthe filtrate was evaporated to dryness
  6. dissolutionthe residue re-dissolved in chloroform
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-d264a38a797541b085380ef383a4575e
출처 데이터셋
uspto-grants-1981_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04267327

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