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Ethyl 4-piperidinecarboxylate → Ethyl 1-(2,2,2-trifluoro-1-(3-(trifluoromethyl)phenyl)ethyl)piperidine-4-carboxylate

HRID 1897965
ノート
印刷プレビュー

反応式

HRID 1897965 の反応式
[F:1][C:2]([F:16])([F:15])[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1)=O.[NH:17]1[CH2:27][CH2:26][CH:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:19][CH2:18]1.C([BH3-])#N.[Na+].C(=O)(O)[O-].[Na+]>ClCCl.CO.[Ti](Cl)(Cl)(Cl)Cl.C(OCC)(=O)C.C1(C)C=CC=CC=1.C(N(CC)CC)C>[F:1][C:2]([F:16])([F:15])[CH:3]([N:17]1[CH2:27][CH2:26][CH:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:19][CH2:18]1)[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

11

反応物 4

HCID 70770Ethyl 4-piperidinecarboxylateHCID 1365592,2,2-Trifluoro-3'-(trifluoromethyl)acetophenoneHCID 516892Sodium BicarbonateHCID 5003444Sodium cyanoborohydride

生成物 1

HCID 86649627Ethyl 1-(2,2,2-trifluoro-1-(3-(trifluoromethyl)phenyl)ethyl)piperidine-4-carboxylate

試薬・触媒・溶媒 6

HCID 24193
Titanium Tetrachloride
触媒
HCID 887Methanol溶媒
HCID 1140Toluene溶媒
HCID 6344Dichloromethane溶媒
HCID 8471Triethylamine溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of 0.355 ml of 2,2,2-trifluoro-1-(3-(trifluoromethyl)phenyl)ethanone in 12 ml of dichloromethane were added 0.32 ml of ethyl isonipecotate, 0.58 ml of triethylamine and 1.05 ml of a toluene solution containing 1 M titanium(IV) chloride at room temperature, followed by stirring the reaction mixture at room temperature overnight. To the reaction mixture was added a solution of 392 mg of sodium cyanoborohydride in 5 ml of methanol at room temperature, followed by stirring the reaction mixture at room temperature for 6 hours. Ethyl acetate and saturated aqueous sodium bicarbonate solution were added to the reaction mixture. An insoluble matter was filtered off using Celite. The ethyl acetate layer was separated, washed with brine, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated in vacuo. The resulting residue was purified by a silica gel column chromatography (eluent: hexane to hexane/ethyl acetate=4/1) to give the title compound as a yellow oil.

後処理

  1. stirringby stirring the reaction mixture at room temperature for 6 hours
  2. filtrationAn insoluble matter was filtered off
  3. customThe ethyl acetate layer was separated
  4. washwashed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated in vacuo
  8. customThe resulting residue was purified by a silica gel column chromatography (eluent: hexane to hexane/ethyl acetate=4/1)

出典と根拠

ORDレコード
ord-0d332d6174b84c70b4e2fbdbd85b866a
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08519136B2

反応ノート

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