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Nitric Acid → tetrahydro-2H-pyran-3-ol nitrate

HRID 1995471
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HRID 1995471 반응식
[N+:1]([O-:4])([OH:3])=[O:2].[O:5]1[CH2:10][CH2:9][CH2:8][CH:7](O)[CH2:6]1>C(OC(=O)C)(=O)C>[N+:1]([O:4][CH:7]1[CH2:8][CH2:9][CH2:10][O:5][CH2:6]1)([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 12256033tetrahydro-2H-pyran-3-ol

생성물 1

HCID 13224378tetrahydro-2H-pyran-3-ol nitrate

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

In a reaction vessel was placed 50 ml acetic anhydride. While cooling, 14 ml of 90 percent fuming nitric acid was added. Following this, 25 g of tetrahydro-2H-pyran-3-ol was added dropwise at -8° to -10° C. over a one hour period. Stirring was continued for 1.5 hours at -10° C. The mixture was then allowed to warm to room temperature and then poured into an ice-water mixture. The organic phase settled and was separated. The organic phase was diluted with methylene chloride and also washed with aqueous NaHCO3 and dried over MgSO4. The solvent was removed under vacuum leaving 24.04 g of tetrahydro-2H-pyran-3-ol nitrate. The structure was confirmed by IR and NMR analysis.

후처리

  1. customIn a reaction vessel was placed
  2. temperatureWhile cooling
  3. additionwas added dropwise at -8° to -10° C. over a one hour period
  4. customwas separated
  5. additionThe organic phase was diluted with methylene chloride
  6. washalso washed with aqueous NaHCO3
  7. dry with materialdried over MgSO4
  8. customThe solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-98cd71fc582d42829c733a3fb4a2c434
출처 데이터셋
uspto-grants-1983_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04405333

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