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Benzoic acid, 2-iodo-, methyl ester → Methyl 2-(3-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-oxopropyl)benzoate

HRID 249040
ノート
印刷プレビュー

反応式

HRID 249040 の反応式
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([CH:12]=[CH:13][C:14]3[CH:15]=[C:16]([CH:20]([OH:23])[CH:21]=[CH2:22])[CH:17]=[CH:18][CH:19]=3)=[N:9]2)=[CH:4][CH:3]=1.[Li]OC(C)=O.O.O.[Li+].[Cl-].I[C:34]1[CH:43]=[CH:42][CH:41]=[CH:40][C:35]=1[C:36]([O:38][CH3:39])=[O:37]>[N+](CCCC)(CCCC)(CCCC)CCCC.[Cl-].CN(C=O)C.CC([O-])=O.CC([O-])=O.[Pd+2]>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([CH:12]=[CH:13][C:14]3[CH:15]=[C:16]([C:20](=[O:23])[CH2:21][CH2:22][C:34]4[CH:43]=[CH:42][CH:41]=[CH:40][C:35]=4[C:36]([O:38][CH3:39])=[O:37])[CH:17]=[CH:18][CH:19]=3)=[N:9]2)=[CH:4][CH:3]=1
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

8

反応物 4

HCID 69132Benzoic acid, 2-iodo-, methyl esterHCID 433294Lithium ChlorideHCID 534062851-(3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl)-2-propen-1-olHCID 178526966lithium;acetate;dihydrate

生成物 1

HCID 53394881Methyl 2-(3-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-oxopropyl)benzoate

試薬・触媒・溶媒 3

HCID 70681
Tetrabutylammonium Chloride
触媒
HCID 167845palladium(II) acetate触媒
HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

A degassed suspension of the product of Step 1 (50.3 g, 156 mmol), n-Bu4NCl (86.0 g, 312 mmol), LiOAc.2H2O (41.2 g, 390 mmol), LiCl (6.84 g, 156 mmol), Pd(OAc)2 (1.00 g, 4.7 mmol), and methyl 2-iodobenzoate (41.00 g, 156 mmol) in DMF (300 mL) was stirred for 3 hours at 90° C. The dark red solution was then cooled to r.t. and poured into 2 L of ice cold H2O. The product was extracted with hot EtOAc, dried over Na2SO4, filtered and concentrated to dryness. It was dissolved in 600 ml of hot toluene and filtered through a small silica pad (1 L). The title product was finally recrystallized from EtOAc:hexane 1:1 (1.2 L). The title product was finally recrystallized from EtOAc:hexane 1:1 (1.2 L). Recrystallization of the mother liquors in EtOAc:hexane 1:3 ( 400 mL) afforded a second crop of the title compound.

後処理

  1. temperatureThe dark red solution was then cooled to r.t.
  2. extractionThe product was extracted with hot EtOAc
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated to dryness
  6. dissolutionIt was dissolved in 600 ml of hot toluene
  7. filtrationfiltered through a small silica pad (1 L)
  8. customThe title product was finally recrystallized from EtOAc:hexane 1:1 (1.2 L)
  9. customThe title product was finally recrystallized from EtOAc:hexane 1:1 (1.2 L)
  10. customRecrystallization of the mother liquors in EtOAc:hexane 1:3 ( 400 mL)

出典と根拠

ORDレコード
ord-2d1b4dea5a214a1abaeccd00afac8b2a
出典データセット
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05212180

反応ノート

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