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Diisopropylethylamine → 3-[2-Methoxy-4-(2-trimethylsilanyl-ethylsulfanyl)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

HRID 503912
ノート
印刷プレビュー

反応式

HRID 503912 の反応式
[CH2:1]([Si:3]([CH2:9]C)([CH2:7]C)[CH2:4][CH2:5][SH:6])C.CCN(C(C)C)C(C)C.[C:20]([O:24][C:25]([N:27]1[CH2:31][CH2:30][CH:29]([C:32]2[CH:37]=[CH:36][C:35](Br)=[CH:34][C:33]=2[O:39][CH3:40])[CH2:28]1)=[O:26])([CH3:23])([CH3:22])[CH3:21].OS([O-])(=O)=O.[K+].[O-]S([O-])(=O)=O.[Na+].[Na+]>O1CCOCC1.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].C1(P(C2C=CC=CC=2)C2C3OC4C(=CC=CC=4P(C4C=CC=CC=4)C4C=CC=CC=4)C(C)(C)C=3C=CC=2)C=CC=CC=1>[C:20]([O:24][C:25]([N:27]1[CH2:31][CH2:30][CH:29]([C:32]2[CH:37]=[CH:36][C:35]([S:6][CH2:5][CH2:4][Si:3]([CH3:1])([CH3:7])[CH3:9])=[CH:34][C:33]=2[O:39][CH3:40])[CH2:28]1)=[O:26])([CH3:23])([CH3:22])[CH3:21]
参加物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 81531DiisopropylethylamineHCID 205579Ethanethiol, 2-(triethylsilyl)-HCID 668773131-Boc-3-(4-bromo-2-methoxyphenyl)pyrrolidineHCID 86586342KHSO4 Na2SO4

生成物 1

HCID 668782423-[2-Methoxy-4-(2-trimethylsilanyl-ethylsulfanyl)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester収率 66.1%

試薬・触媒・溶媒 3

HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)触媒
HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 312751,4-Dioxane溶媒

実験手順

Tris(dibenzylideneacetone)dipalladium(0) (32 mg, 0.03509 mmol), 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene (40 mg, 0.07017 mmol), 2-(triethylsilyl)ethanethiol (57 μL, 1.403 mmol) and DIPEA (0.257 mL, 2.807 mmol) were added to a solution of 3-(4-bromo-2-methoxy-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.50 g, 1.403 mmol) in 1,4-dioxane (10 mL). The reaction mixture was heated at reflux for 18 hours. The reaction mixture was cooled and a solution of 10% KHSO4/Na2SO4 was added. The resulting mixture was extracted with EtOAc, and the combined organic extracts were washed with water and brine; dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc, 95/5) to give 0.380 g (66% yield) of 3-[2-methoxy-4-(2-trimethylsilanyl-ethylsulfanyl)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester as a clear oil.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 18 hours
  3. temperatureThe reaction mixture was cooled
  4. extractionThe resulting mixture was extracted with EtOAc
  5. washthe combined organic extracts were washed with water and brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. customevaporated under reduced pressure
  9. customThe residue was purified via flash chromatography (hexane/EtOAc, 95/5)

出典と根拠

ORDレコード
ord-dfec158e88aa47178396c8315a09528e
出典データセット
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07776910B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート