반응 #4602

ord-45c157a66bd1401c8d8bebfdf83470d2

반응 방정식

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

반응 조건

온도
95°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타rose to about 60° C.
  2. 2
    workup.WAITthen exothermed to about 130° C. in a few seconds
  3. 3
    기타receded to about 40° C.
  4. 4
    workup.STIRRINGThe reaction mixture was stirred
  5. 5
    온도After cooling the reaction mixture to RT
  6. 6
    workup.ADDITIONwas added
  7. 7
    workup.STIRRINGThe reaction mixture was stirred
  8. 8
    온도heated to 90° C. for 0.5 hr
  9. 9
    온도then cooled to RT
  10. 10
    기타The reaction mixture was partitioned between 400 ml of ice water and 400 ml of ether
  11. 11
    기타The organic layer was dried
  12. 12
    농축concentrated in vacuo

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04727072uspto-grants-1988_02