تفاعل #49084

ord-6eda01cc9ea94c74a9311bbfab88dd4c

معادلة التفاعل

[N-]=C=O
Isocyanate
[C-]#N.[K+]
potassium cyanide
CC1CCCN1
2-(RS)-methylpyrrolidine
CC(C)=O
acetone
CC1CCCN1C(C)(C)C#N
title compound
المردود 37.5%
CC1CCCN1C(C)(C)C#N
2-Methyl-2-(2-methyl-1-pyrrolidinyl)propanenitrile
المردود 37.5%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةTo a stirred, ice-cooled
  2. 2
    أخرىthe crude reaction mixture
  3. 3
    استخلاصwas extracted with diethyl ether (2×200 ml)
  4. 4
    غسيلthe combined extracts washed with brine (200 ml)
  5. 5
    تجفيفdried (Na2SO4)
  6. 6
    أخرىevaporated under reduced pressure
  7. 7
    أخرىto afford a pale yellow oil
  8. 8
    workup.STIRRINGThe mixture was stirred for 3 hours
  9. 9
    ترشيحfiltered
  10. 10
    أخرىthe filtrate evaporated

الإجراء التجريبي

To a stirred, ice-cooled mixture of 2-(RS)-methylpyrrolidine (4.25 g; 0.05 mol) and acetone (3.67 ml; 0.05 mol) was added a solution of potassium cyanide (3.25 g; 0.05 mol) in water (25 ml) dropwise over 10 min. After stirring at room temperature overnight, the crude reaction mixture was extracted with diethyl ether (2×200 ml) and the combined extracts washed with brine (200 ml), dried (Na2SO4) and evaporated under reduced pressure to afford a pale yellow oil. This was dissolved in DCM and PS-Isocyanate (4.5 g of resin loading 1.53 mmol/g) added. The mixture was stirred for 3 hours, filtered and the filtrate evaporated to afford the title compound as a colourless semi-solid (2.82 g; 37.5%). 1H NMR (CDCl3) δ(inter alia): 1.10 (3H, d), 1.45 (3H, s), 1.55 (3H, s), 1.75-2.00 (4H, m) 2.65 (1H, m) and 3.05-3.20 (2H, m).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745642B2uspto-grants-2010_06