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Ammonium Chloride → 1,5-Dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one

HRID 651929
ノート
印刷プレビュー

反応式

HRID 651929 の反応式
Br[CH:2]1[C:8](=[O:9])[CH:7](Br)[C:6]2([CH3:12])[O:11][C:3]1([CH3:13])[CH:4]=[CH:5]2.[Cl-].[NH4+]>[Zn].[Cu]>[CH3:12][C:6]12[O:11][C:3]([CH3:13])([CH:4]=[CH:5]1)[CH2:2][C:8](=[O:9])[CH2:7]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 25517Ammonium ChlorideHCID 13534068HCID 13534068、化合物

生成物 1

HCID 135340701,5-Dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one収率 82.6%

試薬・触媒・溶媒 1

HCID 10290809Zinc copper couple触媒

実験手順

To a stirred slurry of 2,4-dibromo-1,5-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (18.0 g) in a saturated methanolic solution of ammonium chloride (514 ml) was added portionwise zinc/copper couple (51 g) over 30 minutes at 23° C. The suspension was stirred for an additional 2 hours and filtered. The filtrate was diluted with a saturated Na2H2 -ethylenediaminetetraacetic acid solution (400 ml). Extraction with methylene chloride (5×100 ml) and drying (MgSO4) produced, upon evaporative removal of solvent, the desired ketone (9.0 g). Bulb-to-bulb distillation <80° C. and 0.5 mm afforded the desired product (7.3 g) as colorless crystals, m.p. 62°-63° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationfiltered
  2. additionThe filtrate was diluted with a saturated Na2H2 -ethylenediaminetetraacetic acid solution (400 ml)
  3. extractionExtraction with methylene chloride (5×100 ml)
  4. dry with materialdrying (MgSO4)
  5. customproduced, upon evaporative removal of solvent
  6. distillationBulb-to-bulb distillation <80° C. and 0.5 mm

出典と根拠

ORDレコード
ord-2ec5614a0aed49f7b8b870af1bf30502
出典データセット
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04670041

反応ノート

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