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Diethyl Ether → (2S,5S)-2-(4'-octyloxycarbonylbenzyloxy)-5-hexyl-delta-valerolactone

HRID 893253
ノート
印刷プレビュー

反応式

HRID 893253 の反応式
Br[CH2:2][C:3]1[CH:19]=[CH:18][C:6]([C:7]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])=[O:8])=[CH:5][CH:4]=1.[OH:20][C@H:21]1[CH2:27][CH2:26][C@@H:25]([CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[O:24][C:22]1=[O:23].C(OCC)C>CN(C)C=O.[Ag]=O>[CH2:10]([O:9][C:7]([C:6]1[CH:18]=[CH:19][C:3]([CH2:2][O:20][C@H:21]2[CH2:27][CH2:26][C@H:25]([CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[O:24][C:22]2=[O:23])=[CH:4][CH:5]=1)=[O:8])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]
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 3

HCID 3283Diethyl EtherHCID 14645393(2S,5R)-hydroxy-5-hexyl-delta-valerolactoneHCID 19891718Octyl p-bromomethylbenzoate

生成物 1

HCID 22844672(2S,5S)-2-(4'-octyloxycarbonylbenzyloxy)-5-hexyl-delta-valerolactone収率 2.2%

試薬・触媒・溶媒 2

HCID 92152Silver(II) oxide触媒
HCID 6228
Dimethylformamide
溶媒

実験手順

In 1.5 ml of dry dimethylformamide were dissolved 180 mg of octyl p-bromomethylbenzoate and 100 mg of (2S,5R)-2-hydroxy-5-hexyl-δ-valerolactone, and 300 mg of silver oxide was added to the solution and the mixture was stirred overnight at room temperature to effect reaction. After the reaction, diethyl ether was added to the reacted solution to extract the reaction product. The extract was washed with a saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate. Diethyl ether was removed by distillation under a reduced pressure. The obtained crude product was purified by the silica gel column chromatography to obtain 5 mg of (2S,5S)-2-(4'-octyloxycarbonylbenzyloxy)-5-hexyl-δ-valerolactone.

後処理

  1. additionwas added to the solution
  2. customreaction
  3. additionwas added to the reacted solution
  4. extractionto extract the reaction product
  5. washThe extract was washed with a saturated aqueous solution of sodium chloride
  6. dry with materialdried on anhydrous magnesium sulfate
  7. customDiethyl ether was removed by distillation under a reduced pressure
  8. customThe obtained crude product
  9. customwas purified by the silica gel column chromatography

出典と根拠

ORDレコード
ord-b48a4ea2f39144efb591a471b81abbd8
出典データセット
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05124069

反応ノート

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