Ammonia → 2-(Cyclohex-1-enyl)-2-aminoethanenitrile

HRID 1242634노트

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HRID 1242634 반응식
[C-:1]#[N:2].[K+].[Cl-].[NH4+:5].N.[C:7]1([CH:13]=O)[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]=1>O.CCOCC>[C:7]1([CH:13]([NH2:5])[C:1]#[N:2])[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]=1

참가 물질

7

실험 절차

In a flask fitted with a mechanical stirrer, a condenser and a dropping funnel was place potassium cyanide (8.45 g, 0.13 mol) and ammonium chloride (7.65 g, 0.143 mol) in water (40 mL). To this solution was added 25 mL of concentrated ammonia. A solution of cyclohex-1-enecarboxaldehyde (14.3 g, 0.13 mol) in ether (100 mL) was added at room temperature with vigorous stirring. Stirring was continued for 3 days and then the layers were separated and the aqueous layer was extracted with ether (50 mL). The combined ether layers were washed with brine (50 mL) and evaporated under reduced pressure to give 15.5 g of an oil. The oil was dissolved in dichloromethane (100 mL) and extracted with 3 M hydrochloric acid (3×30 mL). The acidic extracts were cooled in an ice bath and basified with 75 mL of concentrated ammonia solution. Extraction with dichloromethane (50 mL) afforded 7.8 g (44%) of the title compound as an oil. NMR (CDCl3) δ 6.0–6.3(s br, 1H), 4.0–4.4(S br, 1H), 2.0–2.4(m, 4H), 1.3–2.0(m, 4H),

후처리

  1. customIn a flask fitted with a mechanical stirrer, a condenser and a dropping funnel
  2. customthe layers were separated
  3. extractionthe aqueous layer was extracted with ether (50 mL)
  4. washThe combined ether layers were washed with brine (50 mL)
  5. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-7476ac370aff45af8659e9c99f20a985
출처 데이터셋
uspto-grants-2006_10
특허 번호
US07115748B2

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