تفاعل #583780

ord-9c98bbfa8e2c43289cef07d41ded29a0

معادلة التفاعل

OC(O)C(Cl)(Cl)Cl
chloral hydrate
NC(=O)C1CCCCC1
cyclohexane carboxamide
O=C(NC(O)C(Cl)(Cl)Cl)C1CCCCC1
cyclohexyl-N-(2,2,2-trichloro-1-hydroxyethyl)carboxamide
المردود 80.9%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىFirst, cyclohexyl-N-(2,2,2-trichloro-1-hydroxyethyl)carboxamide 3 was synthesized
  2. 2
    أخرىreaction time
  3. 3
    أخرىremoved from the oil bath
  4. 4
    workup.WAITleft at room temperature
  5. 5
    درجة الحرارةUpon cooling
  6. 6
    أخرىthe crystalline solid formed
  7. 7
    ترشيحwas filtered
  8. 8
    غسيلwashed with hexanes

الإجراء التجريبي

First, cyclohexyl-N-(2,2,2-trichloro-1-hydroxyethyl)carboxamide 3 was synthesized as follows. A mixture of chloral hydrate (9.0 g, 54,5 mmol) and cyclohexane carboxamide (5.0 g, 49.5 mmol) in dry benzene (30 ml) was heated at 80° C. in an oil bath. The initial suspension eventually became a clear solution (reaction time depends on the amount of starting materials, in this example it took about 6 hours). The mixture was stirred for an additional 30 minutes, then removed from the oil bath, and left at room temperature. Upon cooling, the crystalline solid formed was filtered and washed with hexanes to give the product cyclohexyl-N-(2,2,2-trichloro-1-hydroxyethyl)carboxamide 3 (11.0 g). NMR (1H, CDCl3): δ 6.23 (d, J=8.4 Hz, 1H), 5.9 (dd, 1H), 4.35 (broad s, 1H), 2.16 (t, 1H), 1.90-1.22 (m, 10H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06946474B2uspto-grants-2005_09