Hydrochloric Acid → 4,5-Dichloro-2-({3-chloro-2,4-dihydroxy-5-[4-(methoxycarbonyl)butyl]phenyl}carbonyl)benzoic Acid

HRID 1983426

反応式

HRID 1983426 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[O:10])[O:8][C:6](=[O:7])[C:5]2=[CH:11][C:12]=1[Cl:13].[Al+3].[Cl-].[Cl-].[Cl-].[Cl:18][C:19]1[C:20]([OH:34])=[C:21]([CH2:26][CH2:27][CH2:28][CH2:29][C:30]([O:32][CH3:33])=[O:31])[CH:22]=[CH:23][C:24]=1[OH:25].Cl>C(OCC)(=O)C.ClCCCl>[Cl:13][C:12]1[C:2]([Cl:1])=[CH:3][C:4]([C:9]([OH:8])=[O:10])=[C:5]([C:6]([C:23]2[CH:22]=[C:21]([CH2:26][CH2:27][CH2:28][CH2:29][C:30]([O:32][CH3:33])=[O:31])[C:20]([OH:34])=[C:19]([Cl:18])[C:24]=2[OH:25])=[O:7])[CH:11]=1

参加物

7

反応物 4

HCID 313Hydrochloric Acid2 回HCID 703344,5-Dichlorophthalic anhydrideHCID 6451240Aluminum(III) ChlorideHCID 57712912Methyl 5-(3-chloro-2,4-dihydroxyphenyl)pentanoate

生成物 1

HCID 577129344,5-Dichloro-2-({3-chloro-2,4-dihydroxy-5-[4-(methoxycarbonyl)butyl]phenyl}carbonyl)benzoic Acid収率 69%

試薬・触媒・溶媒 2

HCID 111,2-Dichloroethane溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
-20 °C

実験手順

In a 2 L 3-neck round-bottomed flask equipped with a stir and addition funnel was added 4,5-dichlorophthalic anhydride (7.13 g, 32.9 mmol) followed by dry 1,2-dichloroethane (120 ml). After stirring for 30 minutes AlCl3 (11.4 g, 85.54 mmol) was added and the mixture was stirred for another 30 minutes. To this mixture was added via the addition funnel a solution of 5b (8.5 g, 32.9 mmol) with stirring. The solution in the flask became slightly warm and turned dark. Hydrogen chloride gas evolved for about 10 to 20 minutes. Stirring was continued overnight (15-18 hours) at room temperature. During this time, a tarry precipitate formed. To this mixture was added ice (160 g) and concentrated HCl (80 ml) followed by ethyl acetate (900 ml). The content of the flask was stirred until all the solids have completely dissolved. The mixture was transferred to a 2-liter separatory funnel. The organic layer was washed with about 300 ml of 1 N HCl, 2×200 ml of saturated NaCl and dried over sodium sulfate. The solution was filtered and evaporated to a solid, which was then triturated in 200 ml of dichloromethane for 30 minutes, and then cooled to −20° C. for at about 2 h. The crystalline precipitate was filtered off and washed with 2:1 hexanes/dichloromethane, followed by 4:1 hexanes/dichloromethane, and dried to afford 10.8 g (69%) of the desired benzophenone 14b. 1H NMR (DMSO-d6) δ: 12.44 (s, 1H), 10.3 (br s, 1H), 8.14 (s, 1H), 7.87 (s, 1H), 6.88 (s, 1H), 3.55 (s, 3H), 2.44 (t, J=6.8 Hz, 2H), 2.25 (t, J=6.9 Hz, 2H), 1.40 (m, 4H).

後処理

  1. customIn a 2 L 3-neck round-bottomed flask equipped with
  2. additionaddition funnel
  3. additionwas added
  4. stirringthe mixture was stirred for another 30 minutes
  5. stirringwith stirring
  6. temperatureThe solution in the flask became slightly warm
  7. stirringStirring
  8. custom(15-18 hours)
  9. customat room temperature
  10. customDuring this time, a tarry precipitate formed
  11. stirringThe content of the flask was stirred until all the solids
  12. dissolutionhave completely dissolved
  13. customThe mixture was transferred to a 2-liter separatory funnel
  14. washThe organic layer was washed with about 300 ml of 1 N HCl, 2×200 ml of saturated NaCl
  15. dry with materialdried over sodium sulfate
  16. filtrationThe solution was filtered
  17. customevaporated to a solid, which
  18. customwas then triturated in 200 ml of dichloromethane for 30 minutes
  19. filtrationThe crystalline precipitate was filtered off
  20. washwashed with 2:1 hexanes/dichloromethane
  21. customdried

出典と根拠

ORDレコード
ord-b8a3c6a9633245c5be7b990f15c1c988
出典データセット
uspto-grants-2009_06
特許番号
US07541454B2

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