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Hydrochloric Acid → (1E,6E)-1-(3-fluoro-4-hydroxyphenyl)-7-(3-hydroxy-4-methoxyphenyl)hepta-1,6-diene-3,5-dione

HRID 1854653
ノート
印刷プレビュー

反応式

HRID 1854653 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12](=[O:17])[CH2:13][C:14](=[O:16])[CH3:15])[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].B(OB=O)=O.[F:23][C:24]1[CH:25]=[C:26]([CH:29]=[CH:30][C:31]=1[OH:32])[CH:27]=O.B(OCCCC)(OCCCC)OCCCC.C(N)CCC.Cl.C([O-])(O)=O.[Na+]>C(OCC)(=O)C.[Cl-].[Na+].O>[F:23][C:24]1[CH:25]=[C:26](/[CH:27]=[CH:15]/[C:14](=[O:16])[CH2:13][C:12](=[O:17])/[CH:11]=[CH:10]/[C:4]2[CH:5]=[CH:6][C:7]([O:8][CH3:9])=[C:2]([OH:1])[CH:3]=2)[CH:29]=[CH:30][C:31]=1[OH:32]
参加物実験手順後処理出典と根拠反応ノート

参加物

10

反応物 7

HCID 313Hydrochloric AcidHCID 8007ButylamineHCID 12712Tributyl borateHCID 516892Sodium BicarbonateHCID 518682Boron trioxideHCID 5872503-Fluoro-4-hydroxybenzaldehydeHCID 570849216-(3-Hydroxy-4-methoxyphenyl)hex-5-ene-2,4-dione

生成物 1

HCID 68554859(1E,6E)-1-(3-fluoro-4-hydroxyphenyl)-7-(3-hydroxy-4-methoxyphenyl)hepta-1,6-diene-3,5-dione収率 47.5%

試薬・触媒・溶媒 2

HCID 8857Ethyl Acetate溶媒2 回HCID 57417360Sodium chloride; water溶媒

実験手順

6-(3-Hydroxy-4-methoxyphenyl)hex-5-ene-2,4-dione (20 mg, 85 μmol) and boron trioxide (11 mg, 0.16 mmol) was placed in a 20 mL reaction vessel, and dissolved in 0.4 mL of ethyl acetate. To the stirring solution at 80° C. was added a solution of 3-fluoro-4-hydroxybenzaldehyde (15 mg, 0.11 mmol) and tri-n-butyl borate (25 μL, 93 μmol) in 0.7 mL of ethyl acetate. After being stirred for 2 h at the same temperature, n-butylamine (10 μL, 0.10 mmol) was added with additional stirring for 1 h. The reaction mixture was treated with a 1:1 solution (1 mL) of 1N HCl and brine, and was stirred at 50° C. for 5 min to 1 h (if necessary, the reaction mixture was neutralized by saturated NaHCO3 aqueous solution). The organic layer was purified directly by silica gel column chromatography (eluting with hexane/ethyl acetate or chloroform/methanol) to obtain the title compound as a solid (14.4 mg, 47%).

後処理

  1. additionwas added
  2. stirringwas stirred at 50° C. for 5 min to 1 h (if necessary, the reaction mixture
  3. customThe organic layer was purified directly by silica gel column chromatography (eluting with hexane/ethyl acetate or chloroform/methanol)

出典と根拠

ORDレコード
ord-fe7f81aeb8f748698e22b2b31b329e29
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08962674B2

反応ノート

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