تفاعل #1755450

ord-4f99390ce87f463fb161039acb11fac7

معادلة التفاعل

OCC(F)(F)C(F)F
2,2,3,3-tetrafluoropropan-1-ol
CCN(CC)CC
triethylamine
O=S(=O)(F)C(F)(F)F
Trifluoromethanesulfonyl fluoride
O=S(=O)(OCC(F)(F)C(F)F)C(F)(F)F
2,2,3,3-tetrafluoropropyl trifluoromethanesulfonate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىsealed
  2. 2
    أخرىwas set to −10° C
  3. 3
    أخرىdid not exceed −5° C
  4. 4
    workup.ADDITIONOnce the addition
  5. 5
    workup.ADDITIONThe reaction mix
  6. 6
    غسيلwashed with 2×500 mL portions of water and 1×250 mL portion of 1N HCl
  7. 7
    أخرىThe chloroform solvent was removed by rotary evaporation
  8. 8
    تجفيفThe product was dried over anhydrous magnesium sulfate which
  9. 9
    ترشيحwas then filtered from the product

الإجراء التجريبي

2,2,3,3-tetrafluoropropan-1-ol (244.3 g, 1.85 mol, obtained from Sinochem Corp.), triethylamine (187.2 g, 1.85 mol, obtained from Aldrich Chemical Co.) and 500 mL of chloroform were combined in a 2-liter Parr pressure reactor and sealed. The reactor temperature was set to −10° C. Trifluoromethanesulfonyl fluoride (281.33 g, 1.85 mol, obtained from 3M Company) was added at such a rate that the temperature did not exceed −5° C. Once the addition was complete, the mix was held at −10° C. for 45 minutes. The reaction mix was then emptied and washed with 2×500 mL portions of water and 1×250 mL portion of 1N HCl. GC analysis of the reaction mixture indicated a 97 percent conversion to the product. The chloroform solvent was removed by rotary evaporation. The product was dried over anhydrous magnesium sulfate which was then filtered from the product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07988877B2uspto-grants-2011_08