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

HRID 613360
ノート
印刷プレビュー

反応式

HRID 613360 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 222Ammonia2 回HCID 25517Ammonium ChlorideHCID 5360545SodiumHCID 183273631-(2-Benzyloxyethyl)-4-methyl-2,6,7-trioxabicyclo-[2.2.2]octane

生成物 1

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

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-e9c922c18aeb4c3aaed223d9a876843c
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06008224

反応ノート

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