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Sodium Hydroxide → 3-Cyclohexyl-3-methylaminomethyloxetane

HRID 704156
노트
인쇄 미리보기

반응식

HRID 704156 반응식
[CH:1]1([C:7]2([CH:11]=O)[CH2:10][O:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C([O-])(=O)C.[Na+].Cl.CN.[C:21]([BH3-])#[N:22].[Na+].[OH-].[Na+]>CO>[CH:1]1([C:7]2([CH2:11][NH:22][CH3:21])[CH2:10][O:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 14798Sodium HydroxideHCID 517045Sodium AcetateHCID 5003444Sodium cyanoborohydrideHCID 6364545Methylamine hydrochlorideHCID 200755923-Cyclohexyl-3-formyloxetane

생성물 1

HCID 200755603-Cyclohexyl-3-methylaminomethyloxetane

시약·촉매·용매 1

실험 절차

3-Cyclohexyl-3-formyloxetane (1.7 g) was dissolved in methanol (10 ml) at 25° C. In succession, anhydrous sodium acetate (3.3 g), methylamine hydrochloride (3.4 g) and sodium cyanoborohydride (630 mg) were added, followed by a further volume of methanol (30 ml). The mixture was stirred overnight and then basified with sodium hydroxide solution (1M, 22 ml) to pH9. Ether extraction, washing and drying, followed by evaporation gave 3-cyclohexyl-3-methylaminomethyloxetane as a colourless oil.

후처리

  1. extractionEther extraction
  2. washwashing
  3. customdrying
  4. customfollowed by evaporation

출처 및 근거

ORD 기록
ord-4ab2bc696400457f85850ebfb5c9d34d
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04985582

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 887
Methanol
용매
2회