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Iodine → (S)-methyl 2-(tert-butoxycarbonyl)-3-(4-(trifluoromethyl)phenyl)propanoate

HRID 20022
ノート
印刷プレビュー

反応式

HRID 20022 の反応式
II.[C:3]([O:7][C:8]([C@H:10]([CH2:15]I)[C:11]([O:13][CH3:14])=[O:12])=[O:9])([CH3:6])([CH3:5])[CH3:4].I[C:18]1[CH:23]=[CH:22][C:21]([C:24]([F:27])([F:26])[F:25])=[CH:20][CH:19]=1.C1(P(C2C=CC=CC=2C2C(OC)=CC=CC=2OC)C2CCCCC2)CCCCC1>CN(C=O)C.[Zn].C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[C:3]([O:7][C:8]([C@@H:10]([CH2:15][C:18]1[CH:23]=[CH:22][C:21]([C:24]([F:27])([F:26])[F:25])=[CH:20][CH:19]=1)[C:11]([O:13][CH3:14])=[O:12])=[O:9])([CH3:6])([CH3:5])[CH3:4]
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 807IodineHCID 67993Benzene, 1-iodo-4-(trifluoromethyl)-HCID 112698722-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 86614124(R)-methyl2-(tert-butoxycarbonyl)-3-iodopropanoate

生成物 1

HCID 67270692(S)-methyl 2-(tert-butoxycarbonyl)-3-(4-(trifluoromethyl)phenyl)propanoate

試薬・触媒・溶媒 3

HCID 23994
Zinc
触媒
HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

Iodine (0.0140 g, 0.0553 mmol) was added to zinc (0.542 g, 8.29 mmol) and the solid mixture was heated under vacuum for 10 minutes. The flask was flushed with nitrogen three times and allowed to cool. DMF (0.5 mL, degassed with nitrogen) was added and the suspension was cooled to 0° C. and stirred while (R)-methyl 2-(tert-butoxycarbonyl)-3-iodopropanoate (1.82 g, 5.53 mmol) in DMF (2.8 mL) was added dropwise. The mixture was stirred for 30 minutes at 0° C. and then allowed to come to RT for 30 minutes. 1-Iodo-4-(trifluoromethyl)benzene (1.50 g, 5.53 mmol), tris(dibenzylideneacetone)dipalladium (0.101 g, 0.111 mmol), and dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (S-Phos) (0.182 g, 0.442 mmol) were added. The flask was purged with nitrogen and heated at 40° C. After 3 hours the reaction was allowed to cool and partitioned between EtOAc and an aqueous solution of ˜9:1 saturated ammonium chloride/ammonium hydroxide. The aqueous layer was extracted with EtOAc and the combined organic layers were washed with water, brine, and dried over sodium sulfate. Concentration and purification by silica gel chromatography (6:1 Hexanes/EtOAc) afforded (S)-methyl 2-(tert-butoxycarbonyl)-3-(4-(trifluoromethyl)phenyl)propanoate.

後処理

  1. temperaturethe solid mixture was heated under vacuum for 10 minutes
  2. customThe flask was flushed with nitrogen three times
  3. temperatureto cool
  4. additionDMF (0.5 mL, degassed with nitrogen) was added
  5. additionwas added dropwise
  6. waitto come to RT for 30 minutes
  7. customThe flask was purged with nitrogen
  8. temperatureheated at 40° C
  9. waitAfter 3 hours the reaction was allowed
  10. temperatureto cool
  11. custompartitioned between EtOAc
  12. extractionThe aqueous layer was extracted with EtOAc
  13. washthe combined organic layers were washed with water, brine
  14. dry with materialdried over sodium sulfate
  15. concentrationConcentration and purification by silica gel chromatography (6:1 Hexanes/EtOAc)

出典と根拠

ORDレコード
ord-deac4b6a5b2c4becbb470e5fb1bdccf9
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07745484B2

反応ノート

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