Chlorotrimethylsilane → 4-(8-Phenyl-1,4-dioxaspiro[4.5]dec-8-yl)pyrrolidine hydrochloride

HRID 2422391노트

반응식

HRID 2422391 반응식
C1([Mg][Cl:8])C=CC=CC=1.[Cl-].[NH4+].Cl[Si](C)(C)C.Cl.[C:17]1([C:23]2([CH:33]3[CH2:37][NH:36][CH2:35][CH2:34]3)[CH2:32][CH2:31][C:26]3([O:30][CH2:29][CH2:28][O:27]3)[CH2:25][CH2:24]2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.Cl>C1COCC1>[ClH:8].[C:17]1([C:23]2([CH:33]3[CH2:37][NH:36][CH2:35][CH2:34]3)[CH2:32][CH2:31][C:26]3([O:27][CH2:28][CH2:29][O:30]3)[CH2:25][CH2:24]2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

참가 물질

6

실험 절차

The aminonitrile 8-pyrrolidin-1-yl-1,4-dioxaspiro[4,5]decane-8-carbonitrile (10.0 g, 42.6 mmol), dissolved in THF (90 ml), was added under argon and with ice cooling within 15 min to a 1.82M phenyl magnesium chloride solution in THF (70 ml, 0.127 mol) and the mixture was stirred for 16 h at room temperature. The reaction mixture was processed by adding saturated ammonium chloride solution (100 ml) with ice cooling and was then extracted with diethyl ether (3×100 ml). The organic phase was extracted by shaking with water (70 ml) and saturated NaCl solution (70 ml) and concentrated to small volume. A yellow crystal paste (11.8 g) was retained which in addition to the desired product still contained the ketal 8-pyrrolidin-1-yl-1,4-dioxaspiro[4,5]decane-8-carbonitrile. The crude product was dissolved in ethyl methyl ketone (70 ml) and ClSiMe3 (8 ml, 0.063 mol) was added with ice cooling. After a reaction time of 6 h the hydrochloride 4-(8-phenyl-1,4-dioxaspiro[4,5]dec-8-yl)pyrrolidine hydrochloride was able to be isolated as a white solid in a yield of 43% (5.9 g).

후처리

  1. extractionwas then extracted with diethyl ether (3×100 ml)
  2. extractionThe organic phase was extracted
  3. stirringby shaking with water (70 ml) and saturated NaCl solution (70 ml)
  4. concentrationconcentrated to small volume
  5. additionin addition to the desired product
  6. dissolutionThe crude product was dissolved in ethyl methyl ketone (70 ml)
  7. customAfter a reaction time of 6 h
  8. customto be isolated as a white solid in a yield of 43% (5.9 g)

출처 및 근거

ORD 기록
ord-0281ec7aa5ca4d38968c7050b0abb862
출처 데이터셋
uspto-grants-2011_06
특허 번호
US07960404B2

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