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Ammonia → 1-(2-Hydroxyethyl)-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane

HRID 613360
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HRID 613360 반응식
N.C([O:9][CH2:10][CH2:11][C:12]12[O:19][CH2:18][C:15]([CH3:20])([CH2:16][O:17]1)[CH2:14][O:13]2)C1C=CC=CC=1.[Na].[Cl-].[NH4+]>O1CCCC1>[OH:9][CH2:10][CH2:11][C:12]12[O:13][CH2:14][C:15]([CH3:20])([CH2:16][O:17]1)[CH2:18][O:19]2
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참가 물질

6

반응물 4

HCID 222Ammonia2회HCID 25517Ammonium ChlorideHCID 5360545SodiumHCID 183273631-(2-Benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octane

생성물 1

HCID 183273721-(2-Hydroxyethyl)-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane수율 60%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

To liquid ammonia (35 ml) was added, under an argon atmosphere, a solution of 1-(2-Benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octane (3.54 g) in anhydrous tetrahydrofuran (8 ml). Metallic sodium (500 mg) was then added thereto, and the resultant mixture was stirred for 3 hours at -78° C. After ammonium chloride was added to the reaction mixture, ammonia was evaporated, and tetrahydrofuran was evaporated under reduced pressure. The residue was washed with ether, and the resultant solid was added to saturated brine and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, to give 1-(2-hydroxyethyl)-4-methyl-2,6,7-trioxabicyclo[2.2.2]octane (1.4 g) as a pale yellow oil.

후처리

  1. customwas evaporated
  2. customtetrahydrofuran was evaporated under reduced pressure
  3. washThe residue was washed with ether
  4. additionthe resultant solid was added to saturated brine
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with saturated brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-e9c922c18aeb4c3aaed223d9a876843c
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06008224

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