تفاعل #4602

ord-45c157a66bd1401c8d8bebfdf83470d2

معادلة التفاعل

C1CCNC1
pyrrolidine
[Na+].[OH-]
sodium hydroxide
ClCC1CO1
epichlorohydrin
CC(C)(C)CO
neopentyl alcohol
CC(C)(C)COCC(O)CN1CCCC1
oil
المردود 84.1%
CC(C)(C)COCC(O)CN1CCCC1
α-[(2,2-Dimethylpropoxy)methyl]-1-pyrrolidineethanol
المردود 84.1%

ظروف التفاعل

درجة الحرارة
95°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىrose to about 60° C.
  2. 2
    workup.WAITthen exothermed to about 130° C. in a few seconds
  3. 3
    أخرىreceded to about 40° C.
  4. 4
    workup.STIRRINGThe reaction mixture was stirred
  5. 5
    درجة الحرارةAfter cooling the reaction mixture to RT
  6. 6
    workup.ADDITIONwas added
  7. 7
    workup.STIRRINGThe reaction mixture was stirred
  8. 8
    درجة الحرارةheated to 90° C. for 0.5 hr
  9. 9
    درجة الحرارةthen cooled to RT
  10. 10
    أخرىThe reaction mixture was partitioned between 400 ml of ice water and 400 ml of ether
  11. 11
    أخرىThe organic layer was dried
  12. 12
    تركيزconcentrated in vacuo

الإجراء التجريبي

To a stirred mixture of 92.53 g (1.0 m) of epichlorohydrin and 88.15 g (1.0 m) of neopentyl alcohol was added 0.26 g (0.001 m) of stannic chloride. The reaction temperature rose to about 60° C. then exothermed to about 130° C. in a few seconds. The reaction mixture was stirred until the temperature receded to about 40° C. then 71.12 g (1.0 m) of pyrrolidine was added. The reaction mixture was stirred and heated to about 95° C. for 1 hr. After cooling the reaction mixture to RT, a mixture of 80 g of 50% sodium hydroxide solution and 80 g of ice was added. The reaction mixture was stirred and heated to 90° C. for 0.5 hr then cooled to RT. The reaction mixture was partitioned between 400 ml of ice water and 400 ml of ether. The organic layer was dried and concentrated in vacuo to give 181 g of oil. The oil was distilled (89°-115° C. at 0.25 mm) to give 136 g of oil that crystallized on standing, 99.1% pure by g.c.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04727072uspto-grants-1988_02