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5-Bromo-2-chlorotoluene → Ethyl(3R)-2-(4-chloro-3-methylphenyl)-4,4,4-trifluoro-3-methylbutanoate

HRID 1476110
ノート
印刷プレビュー

反応式

HRID 1476110 の反応式
C[Si](C)(C)[N-][Si](C)(C)C.[Li+].[F:11][C:12]([F:22])([F:21])[C@H:13]([CH3:20])[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16].Br[C:24]1[CH:25]=[CH:26][C:27]([Cl:31])=[C:28]([CH3:30])[CH:29]=1.C1(P(C2CCCCC2)C2C=CC=CC=2C2C=CC=CC=2N(C)C)CCCCC1>C1(C)C=CC=CC=1.C(OCC)(=O)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[Cl:31][C:27]1[CH:26]=[CH:25][C:24]([CH:14]([C@@H:13]([CH3:20])[C:12]([F:21])([F:22])[F:11])[C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:29][C:28]=1[CH3:30]
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 6098995-Bromo-2-chlorotolueneHCID 2733832Lithium hexamethyldisilazaneHCID 27342172-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 6992847Ethyl(3R)-4,4,4-trifluoro-3-methylbutanoate

生成物 1

HCID 58288443Ethyl(3R)-2-(4-chloro-3-methylphenyl)-4,4,4-trifluoro-3-methylbutanoate

試薬・触媒・溶媒 3

HCID 167845
palladium(II) acetate
触媒
HCID 1140Toluene溶媒3 回
HCID 8857Ethyl Acetate溶媒

反応条件

温度
-10 °C

実験手順

29.2 ml (29.2 mmol) of a 1 M solution of lithium hexamethyldisilazide in toluene were cooled to −10° C., and a solution of 4.30 g (23.4 mmol) of ethyl (3R)-4,4,4-trifluoro-3-methylbutanoate in 26 ml of abs. toluene was added dropwise. The mixture was stirred for 10 min At −10° C., a solution, prepared beforehand, of 5.0 g (19.5 mmol, 80% pure) of 5-bromo-2-chlorotoluene, 131 mg (0.58 mmol) of palladium(II) acetate and 483 mg (1.23 mmol) of 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl in 26 ml of abs. toluene was then added dropwise. The resulting reaction mixture was initially stirred at RT for 1 h and then at 80° C. for 4 h. After cooling, the mixture was diluted with ethyl acetate, washed twice with sat. aqueous sodium bicarbonate solution and once with sat. sodium chloride solution, dried over sodium sulphate and concentrated under reduced pressure. This gave 7.80 g of the title compound as a crude product which was directly reacted further.

後処理

  1. customa solution, prepared beforehand
  2. customThe resulting reaction mixture
  3. stirringwas initially stirred at RT for 1 h
  4. waitat 80° C. for 4 h
  5. temperatureAfter cooling
  6. washwashed twice with sat. aqueous sodium bicarbonate solution and once with sat. sodium chloride solution
  7. dry with materialdried over sodium sulphate
  8. concentrationconcentrated under reduced pressure
  9. customThis gave 7.80 g of the title compound as a crude product which was directly reacted further

出典と根拠

ORDレコード
ord-19995d48ae1d4fa994c5d8125423e647
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09018414B2

反応ノート

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