Sodium Acetate → 1,2,6,7-Tetrahydro-8H-indeno[5,4-b]furan-8-one

HRID 420900ノート

反応式

HRID 420900 の反応式
Br[C:2]1[C:10]2[O:11][CH2:12][CH2:13][C:9]=2[C:8]2[C:7](=[O:14])[CH2:6][CH2:5][C:4]=2[C:3]=1Br.C([O-])(=O)C.[Na+].[H][H]>[Pd].CO>[CH2:13]1[CH2:12][O:11][C:10]2[CH:2]=[CH:3][C:4]3[CH2:5][CH2:6][C:7](=[O:14])[C:8]=3[C:9]1=2

参加物

6

反応物 3

HCID 517045Sodium AcetateHCID 117272814,5-Dibromo-1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-oneHCID 178418361HCID 178418361、化合物

生成物 1

HCID 111376161,2,6,7-Tetrahydro-8H-indeno[5,4-b]furan-8-one収率 86.6%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

4,5-Dibromo-1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-one (280 kg, 843 mol), anhydrous sodium acetate (173 kg, 2109 mol), methanol (6384 L) were mixed, and the reaction system was replaced with nitrogen. Then, to the reaction mixture was added 10% Pd/C (30.8 kg, as dry weight), and pressurized with hydrogen to 0.29 to 0.49 MPa, and catalytically reduced at about 40° C. for 8 hrs with stirring at such a stirring rate that the gas-liquid overall mass transfer coefficient KLa(1/hr) is about 15. The catalyst was filtered, and the filtrate was concentrated under reduced pressure, and further water was added to the residue, followed by concentrating under reduced pressure to substitute the solvent, cooling and stirring for 1 hr to mature. The crystallization solution was filtered to give wet crystals of title compound (amount 127 kg as dry weight, yield 86.6%). The content of dimer in the wet crystals was less than 0.1% by weight. (2) Purification Step

後処理

  1. filtrationThe catalyst was filtered
  2. concentrationthe filtrate was concentrated under reduced pressure, and further water
  3. additionwas added to the residue
  4. concentrationby concentrating under reduced pressure
  5. temperaturecooling
  6. stirringstirring for 1 hr
  7. filtrationThe crystallization solution was filtered

出典と根拠

ORDレコード
ord-c70c8df87e32428fbe516f9630772ea8
出典データセット
uspto-grants-2012_01
特許番号
US08097737B2

反応ノート

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