Triethylamine → 2-Nitrobenzyl perfluorooctanoate

HRID 1111552

Reaction equation

HRID 1111552 reaction equation
[F:1][C:2]([F:25])([C:6]([F:24])([F:23])[C:7]([F:22])([F:21])[C:8]([F:20])([F:19])[C:9]([F:18])([F:17])[C:10]([F:16])([F:15])[C:11]([F:14])([F:13])[F:12])[C:3](Cl)=[O:4].[N+:26]([C:29]1[CH:36]=[CH:35][CH:34]=[CH:33][C:30]=1[CH2:31][OH:32])([O-:28])=[O:27].C(N(CC)CC)C.Cl.C(N(CC)CC)C>C1C=CC=CC=1>[F:1][C:2]([F:25])([C:6]([F:24])([F:23])[C:7]([F:22])([F:21])[C:8]([F:20])([F:19])[C:9]([F:18])([F:17])[C:10]([F:16])([F:15])[C:11]([F:14])([F:13])[F:12])[C:3]([O:32][CH2:31][C:30]1[CH:33]=[CH:34][CH:35]=[CH:36][C:29]=1[N+:26]([O-:28])=[O:27])=[O:4]

Participants

6

Procedure

Perfluorooctanoyl chloride (21.6 g, 0.05 mol) was added slowly with stirring to a solution of 2-nitrobenzyl alcohol (7.65 g, 0.05 mol) and triethylamine (5.2 g, 0.05 mol) in 100 ml benzene. During the addition, the temperature was allowed to rise to 50° C. and the triethylamine hydrochloride began to precipitate. After the addition was complete, the reaction was stirred an additional 30 minutes. The reaction was filtered and the filtrate evaporated in vacuo to give an oil which crystallized on cooling in an ice bath (m.p. 34°-35° C.). Benzene washings of the material retained on the filter paper gave a second fraction of oil which crystallized on cooling. Total yield was 11.97 g.

Workup

  1. additionDuring the addition
  2. customto rise to 50° C.
  3. customto precipitate
  4. additionAfter the addition
  5. filtrationThe reaction was filtered
  6. customthe filtrate evaporated in vacuo
  7. customto give an oil which
  8. customcrystallized
  9. temperatureon cooling in an ice bath (m.p. 34°-35° C.)
  10. customgave a second fraction of oil which
  11. customcrystallized
  12. temperatureon cooling

Sources & evidence

ORD record
ord-90dad4268b454d1e82866a9156e0c4f0
Source dataset
uspto-grants-1990_12
Patent number
US04980096

Linked notes

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