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1,2-Dimethoxyethane → 3-Vinyl-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine

HRID 656865
ノート
印刷プレビュー

反応式

HRID 656865 の反応式
Cl[C:2]1[N:7]=[N:6][C:5]2[O:8][CH2:9][CH2:10][O:11][C:4]=2[CH:3]=1.[CH2:12]([CH2:15]OC)OC>>[CH:12]([C:2]1[N:7]=[N:6][C:5]2[O:8][CH2:9][CH2:10][O:11][C:4]=2[CH:3]=1)=[CH2:15]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 80711,2-DimethoxyethaneHCID 552674403-Chloro-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine

生成物 1

HCID 675264353-Vinyl-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine収率 50%

反応条件

温度
95 °C

実験手順

A solution of 3-chloro-6,7-dihydro[1,4]dioxino[2,3-c]pyridazine (13.6 g, 0.079 mol) containing ca. 15% of a bromo species in dimethoxyethane (400 ml) was degassed under argon for 10 min then tetrakis(triphenylphosphine)palladium (0) (2 g), potassium carbonate (10.33 g), 2,4,6-trivinylcyclotriboroxane pyridine complex (11.32 g) and water (55 ml) were added. The mixture was heated at 95° C. for 48 hours and cooled and evaporated to dryness. The mixture was treated with aqueous sodium bicarbonate solution and extracted (5×) with DCM. Extracts were dried (sodium sulphate), evaporated and the residue chromatographed on silica gel (500 g), eluting with 0-100% ethyl acetate-hexane, affording the product (6.43 g, 50%); [also some impure fractions (1.8 g)].

後処理

  1. customwas degassed under argon for 10 min
  2. additiontetrakis(triphenylphosphine)palladium (0) (2 g), potassium carbonate (10.33 g), 2,4,6-trivinylcyclotriboroxane pyridine complex (11.32 g) and water (55 ml) were added
  3. temperaturecooled
  4. customevaporated to dryness
  5. additionThe mixture was treated with aqueous sodium bicarbonate solution
  6. extractionextracted (5×) with DCM
  7. dry with materialExtracts were dried (sodium sulphate)
  8. customevaporated
  9. customthe residue chromatographed on silica gel (500 g)
  10. washeluting with 0-100% ethyl acetate-hexane

出典と根拠

ORDレコード
ord-d868b99f3b41424dbc4ec05e98d1b9ee
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08071592B2

反応ノート

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