Diethyl Ether → beta-Ethenylidene-2-thiopeneethanamine

HRID 231557노트

반응식

HRID 231557 반응식
CC[O:3]CC.C[Si](C)(C)[N:8]([CH2:13][C:14]#[C:15][CH2:16]OC)[Si](C)(C)C.[S:21]1[CH:25]=[CH:24][CH:23]=[C:22]1[Mg]Br.[NH4+].[OH-]>Cl[Ni]Cl.C(OC(=O)C)C>[NH4+:8].[OH-:3].[C:15](=[C:14]([C:22]1[S:21][CH:25]=[CH:24][CH:23]=1)[CH2:13][NH2:8])=[CH2:16]

참가 물질

8

반응물 4

HCID 3283Diethyl EtherHCID 14923Ammonium HydroxideHCID 13161121N,N-bis(trimethylsilyl)-4-methoxy-2-butynylamineHCID 178418438HCID 178418438, 화합물

생성물 2

HCID 14923Ammonium HydroxideHCID 14518110beta-Ethenylidene-2-thiopeneethanamine수율 87%

시약·촉매·용매 2

HCID 24385Nickel Dichloride촉매HCID 8857Ethyl Acetate용매

실험 절차

NiCl2 (dppp) catalyst (170 mg; 3M %) was added to dry ether (30 ml) in a 100 ml 3-necked flask with mechanical stirrer, thermometer and nitrogen bubbler. III (2.47g, 10.2 mM) was added via syringe with stirring and immediately thereafter 3M thienylmagnesium bromide (7 ml, 21 mM) was added via syringe. After stirring at room temperature for 20 hours the reaction was complete as shown by G C analysis. The silylated product was isolated by shaking with dilute NH4OH and extraction into ethylacetate (three times, each into 100 ml). After drying over K2CO3 and concentration, 2.68 g crude product was obtained. Purification and desilyation by flash chromatography (300 g silica gel, eluted with CHCl3, then CHCl3 :MeOH:conc. NH4OH 100:10:1) gave 1.22 g (87%) of the desired product as a light tan oil after drying under high vacuum.

후처리

  1. stirringAfter stirring at room temperature for 20 hours the reaction
  2. customThe silylated product was isolated
  3. dry with materialAfter drying over K2CO3 and concentration
  4. custom2.68 g crude product was obtained
  5. customPurification and desilyation by flash chromatography (300 g silica gel
  6. washeluted with CHCl3

출처 및 근거

ORD 기록
ord-1675d6007a9b4d018e3fc7e039de8aac
출처 데이터셋
uspto-grants-1989_07
특허 번호
US04847288

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