تفاعل #1796331

ord-7b42050a3adc4e5c84929e1b53f0d35c

معادلة التفاعل

CCCCc1ccc(C(=O)O)cc1
4-n-butylbenzoic acid
CCCC[C@H]1CC[C@@H](C(=O)O)CC1
cis-4- n-butylcyclohexanecarboxylic acid

المتفاعلات

الكواشف

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe catalyst was filtered
  2. 2
    أخرىthe solution evaporated in vacuo

الإجراء التجريبي

4-n-butylbenzoic acid (8, 50 g, 0.28 mol) was dissolved in glacial acetic acid (250 ml ) and the solution was then autoclaved and hydrogented over platinum oxide (2.0 g) at 20° C. for 18 hr. at 5- p.s.i. The catalyst was filtered and the solution evaporated in vacuo to leave a solid residue of predominantly cis-4- n-butylcyclohexanecarboxylic acid (9, 50.89). The solid was dissolved in dry dichloromethane (250ml) containing N,N-dimethylformamide (1 ml). Thionyl chloride (72.69, 0.61 mol) was cautiously added over 30 min and the mixture was then heated at reflux for 3 hr. The resultant solution was cooled to 20° C., anhydrous ethanol (31.5 g, 0.69 mol) was carefully added and the mixture was then heated at reflux for 1 hr. The cooled solution was poured into water (400 ml) and the separated dichloromethane layer was evaporated to give mainly ethyl cis-4-n-butylcyclohexanecarboxylate (13, 56.4 g), as a viscous oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04948790uspto-grants-1990_08