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

HRID 2233177
ノート
印刷プレビュー

反応式

HRID 2233177 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), triethenylboroxin pyridine complex (11.32 g) and water (55 ml) were added. The mixture was heated at 95° C. for 48 h 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), triethenylboroxin 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-bca3196f050e4950948142be4beab999
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07709483B2

反応ノート

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