Hydrochloric Acid → N,4,4-trimethylcyclohexan-1-amine

HRID 53261

반응식

HRID 53261 반응식
[CH3:1][C:2]1([CH3:9])[CH2:7][CH2:6][C:5](=O)[CH2:4][CH2:3]1.Cl.CN.[C:13]([BH3-])#[N:14].[Na+].Cl>CO>[CH3:13][NH:14][CH:5]1[CH2:6][CH2:7][C:2]([CH3:9])([CH3:1])[CH2:3][CH2:4]1

참가 물질

6

실험 절차

To a solution of 4,4-dimethylcyclohexanone (25.2 g) in dry methanol under an atmosphere of nitrogen was added methylamine hydrochloride (13.2 g) and 3 Åmol sieves (1 g). The reaction mixture was stirred for 1 hr then sodium cyanoborohydride (12.7 g) added portionwise. The mixture was stirred for 17 hrs. A saturated solution of hydrogen chloride in methanol (200 ml) was added and the reaction mixture stirred for 1 hr the filtered through hyflo and concentrated in vacuo. The residue was partitioned between 1N sodium hydroxide (300 ml) and dichloromethane (200 ml). The layers were separated and the aqueous re-extracted with dichloromethane (2×200 ml). The combined organics were washed with saturated sodium hydrogen concentrated in vacuo. The residue was distilled under reduced pressure. Bpt 40°-45° C. at 0.1 mmHg. 1H NMR (CDCl s) δ0.92 (6H, s), 1.10-1.30 (5H, m), 1.30-1.50 (2H, m), 1.66-1.72 (2H, m), 2.26 (1H, m), 2.42 (3H, s).

후처리

  1. stirringThe mixture was stirred for 17 hrs
  2. stirringthe reaction mixture stirred for 1 hr the
  3. filtrationfiltered through hyflo
  4. concentrationconcentrated in vacuo
  5. customThe residue was partitioned between 1N sodium hydroxide (300 ml) and dichloromethane (200 ml)
  6. customThe layers were separated
  7. extractionthe aqueous re-extracted with dichloromethane (2×200 ml)
  8. washThe combined organics were washed with saturated sodium hydrogen
  9. concentrationconcentrated in vacuo
  10. distillationThe residue was distilled under reduced pressure
  11. customBpt 40°-45° C.

출처 및 근거

ORD 기록
ord-7dfc8ddd38c046b0a0691456b7abfb4e
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05618812

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